前苏联专利SU1431680A3 Method of producing 4, 1 prime, 6 prime-trichloro-4,1 prime, 6 prime-tridioxygalactosaccharose

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专利摘要:
A process for the preparation of 4,1',6'-trichloro--4,1',6'-trideoxygalactosucrose (TGS) comprising the steps of: (a) reacting sucrose with an acylating reagent under conditions to provide a mixture of acylated sucrose derivatives containing a major proportion of 6-monoacylated material; (b) optionally separating 6-monoacylated sucrose derivative from other acylated derivatives before step (c); (c) reacting the monoacylated sucrose derivative with a chlorinating reagent capable of chlorinating at positions 1', 4 and 6' of a sucrose 6- acylate; and (d) deacylating and separating (in either order) the 4,1', 6'-trichloro-4, 1', 6'-trideoxygalactosucrose material formed.
公开号:SU1431680A3
申请号:SU813338232
申请日:1981-07-07
公开日:1988-10-15
发明作者:Султан Муфти Хизар；Ахмед Хан Риаз
申请人:Тейт Энд Лайл Паблик Лимитед Компани (Фирма)；
IPC主号:

专利说明:

cm
The invention relates to an improved method for the preparation of A, 1, b trichloro-4 J1, 6 -treexnglaghosachorase (TGS), a known sweetener.
The purpose of the invention is the development of a simplified and more selective method of obtaining TGS and sucrose, carried out through the production of 6-monoacyl ™ a sucrose, with its subsequent chlorination in / 4,1% b - polo I and deactivated
, PRI me R 1 s. Partial aceti-sucrose
Sucrose g is dissolved in pyri-chin 30 ml by boiling for 5 min. The solution is cooled to room temperature, and acetic anhydride 0.606 ml, 1.1 mol. Equiv. Is added to the solution. The reaction mixture is maintained at room temperature: during I h TLC (CHC1, –MeOH 2: 1) shows three fast-moving products, the fastest is obtained in a very small amount, and the rest is two in the mail: the same: quantities “ & 5% also about 2.5% non-procuring sucrose. By this time, all the succes- sive | g-grit is absorbed by the analysis showed that the yield of sucrose b-acetat at this stage is approximately 50%
Chlorination of acetylated sakarosis.
Chloroforc 30 MP is added to the mixture described above. The contents are cooled to -75 ° C in a dry ice bath and; acetone, the loroform is added first: for ipe to tbp, the freezing of pyridine, but also for slowing down the reaction, thus better control of the reaction is achieved. Then, to the cooled reaction mixture, add: dropwise sulphuryl (30 mol, sic) 14L2 MP for lj, 5 h, Zatam reaktioikuk), the mixture is heated to room temperature and left
4h after
for 12 hours and then. About: Gladzhak1T to room temperature.
The mixture is poured into a pre-cooled (pri-4. C) 10%; Sulfuric acid solution (100 cells) slowly with. fmixing The mixture of sulfuric acid is extracted with dna; s chloroform, and & : stract chlorophoric protrusion twice with saturated water
n; pk this temperature for A h, which is heated at 45 ° C
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thief sodium hydrogen carbonate pH 7 and then twice with water, and dried over anhydrous sodium sulfate. The sodium sulfate is filtered off, the filtrate is concentrated to a syrup, and the syrup is dissolved in methanol (50 ml). The methanol solution is then dechlorosulfated with a catalytic amount of Nalj crystals while keeping the solution in an ice bath. Sulfates precipitate. The solution is then neutralized with sodium carbonate. pH 7 and the sulphates and carbonates are filtered off.
The filtrate is then deadatcled with sodium methylate (1 and, up to pH 10 for 4 hours). TLC in ethyl acetate - acetone - water (6: 6: 1) gave TGS and several quickly and medically moving products.
The mixture is then concentrated and eluted from a silica gel column (Merck Kieselgel 60 70–230 mesh ASTM) of about 75 g using chlorine decor - acetone (2: 1) in the nachagge and then chloroform - acetone (: 1) c. as a slurry to obtain the desired TGS in about 15% yield of the initial sucrose.
When the deacetylated syrup is divided between ether and water, most of the products 5 that move faster than TGS go on the air. The aqueous extract is evaporated and subjected to TLC (silica gel) to reveal the presence of from 18 to 22% water-soluble material, like TGS.
In such a reaction, the deacetylated syrup is partitioned between chloroform and water5 and the aqueous layer is evaporated and checked with GGH after silylation. The extract contains approximately 27% TGS and approximately 10% DHS (1 ,., 4-dichloro-2, 4-dideoxy sucrose) "
PRI me R, 2. Sucrose (3., 42 g 10 mmol) and sodium carbonate (3.7 g, 35 mmol) are dissolved in water (60 ml).
A solution of benzoyl chloride (2p9 ml, 25) in dichloromethane (20 ml) is added and the mixture is stirred at room temperature for 2 hours. The aqueous layer is separated and neutralized with diluted HC1 and evaporated to dryness to give a mixture of unreacted sucrose and two monobenoylated compounds (8: 1 ). The mixture of benzoyl-vannc compounds is separated from sucrose by zlation through a column of silica gel (as before Merck Kizel
gel) using the ethyl acetate-acetone-water 10: 10: 1 system.
The mixture of monobenzoate compounds is then chlorinated, using 30 mol. Equiv. sulfuryl chloride, as described in Example 1. After the mixture was sterilized (using 1N methylate to pH 10 for 4 h), it was chromatographed on silica gel.
PRI me R 3, 1. Acetylation.
Sucrose (250 g) and pygridine (3.125 l) are added to a 5-liter flask with a ribbed neck and a round bottom, equipped with a stirrer, condenser, and heating grid on top. The mixture is stirred and heated for 20 minutes at the boiling point when dissolved The flask is cooled to room temperature for several hours without stirring, left overnight at room temperature, and then cooled to -35 ° C in an acetone bath. Both the cooling acetone and the contents of the flask are stirred with an overhead stirrer. Acetic anhydride (85 ml, 1.1 mol, eq.) Is added and the temperature is maintained at -30 to -35 ° C for 8 hours. Water is added (20 ml and the reaction system is brought to room temperature overnight.
The reaction mixture is transferred to a 10-liter Buzi flask and concentrated at 50 ° C with a water pump (10-40 mm Hg) for one hour (distillate approximately 3 liters) and under high vacuum (5-10 mm Hg) for one hour with obtaining a product in the form of a sticky solid (about 380 g in weight). Acetone-water mixture (7: 3, 400 ml) is added to the flask, KOTQpyn is heated to 50 ° C and rotated until the dissolution is complete. The resulting solution is divided into two equal parts of approximately 360 ml, and the Bukhi flask is washed with another volume of approximately 50 m of acetone-water. A sample of this material (approximately 1 ml) is concentrated to a syrup and analyzed to determine the content of sucrose b-acetate (analysis: approximately 40% of 6-acetate saccharide). The remaining material is stored in a corked vial at 4 ° C as long as required.
2. Separation on a column of resin.
Dowex resin, 50-J 00 mesh sukup (cation exchange
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polystyrene sulfonic acid resin based) crosslinked with 4% divinylbenzene, derived from Sigma in the hydrogen form. The resin in the hydrogen form (3.8 kg) is suspended in water to a volume of 6 l. The ammonia solution (S, G, 0.880, 900 ml) is added and gently stirred by hand. There must be an excess of amg-shak. The resin is decanted with demineralized water (4 liters) until ammonia remains. The water is decanted and the resin is mixed with acetone (4 L). The acetone is removed by decantation and the resin is mixed with l of 70% acetone (70 parts of acetone + 30 hours, demineralized water). A glass column GVE cm diameter -jc 100 cm is provided at the top and bottom with thread adapters (B34), the lower cone is provided with a B34 tube and a stopper, and the tube is filled with glass wool to support the resin. The upper cone is equipped with a solvent supply system. The resin slurry is poured and allowed to stand, a) The height of the resin bed is 94 cm, which is a resin volume of 4.4 liters. The column is washed with 70% acetone / water system (20 l) at 50 ml / min.
One part of the acetone-water solution from the process, acetylating the filter, vacuum under vacuum through a glass fiber filter (Whatman GF) (A) into a Buchner flask to remove any traces of bold. The solution is then passed onto the resin surface using an elongated tube separating funnel at such a rate that the resin layer is not damaged and a well-defined layer of sample solution is formed between the solvent and the resin. The flow rate in the column is reduced to 25 ml / min at this stage. After the addition of the sample is completed, the flow rate will increase to 50 5 l / nin.
500 ml fractions are collected, the first fraction is collected immediately as the sample solution reaches the top of the resin. Fractions 1-4 are discarded and the rest is collected and analyzed using those (MeOH 2: 1). 36 fractions were collected with a total volume of 18 l of eluent. These fractions containing the main part of monoacetate: sucrose (usually 12-.0) 3 are concentrated together in a 10-liter flask with a water pump at 50 C. Fractions 11–18 yield 1.95 l at 120–180 mm Hg.
it is released, and the pressure of the water pump drops to 10–20 mm Hg, then another 1.03 liter of distillate is collected.
After the last fraction has been collected, the column is ready for subsequent use without regeneration.
These operations are repeated with the second part of the acetone-water solution from the acetylated stage. The acetone (# 1) is then added to the combined syrup product and distilled off to remove residual water. The resulting white baking is dried in a Buch flask with .f using a vacuum pump (3-5 km I g) for 30 and n Product E3 was taken 8-yr (166 g), then: 3 da1F (150 ml) was dissolved and transferred -: from 500 ml to flask; Bukh flask to add another DMF (.5 ml). : A small sample of DMF solution; concentrated to dryness and analyzed for 6 sucrose acetate using GLC (approximately 85%),
The LOL sieve is added to the DMF solution to remove the last traces of the syringe. After stirring for 1 h, the DIP solution is removed by decantation and the sieve is washed with DMF (w),; Zo Chlorination.
DMF (3 L) to O-C in a 5-liter cup; and add RCC- (2 kg): with agitation and at the temperature of the squeezing medium, while the temperature of the resulting mixture is maintained with ng-kke. 11 After the addition of the mixture in the mixing glass
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nitrogen to alleviate hydrogen chloride. The reaction mixture is then heated and stirred for 1.5 hours at 120 ° C. of the internal temperature (bath temperature is about 126 ° C.) and this temperature is maintained for another 2.5 hours.
During this heating period, the reaction is monitored by TLC (CH, j Cl / MeOH 4: 1), and the sample is pretreated with ammonium hydroxide in methanol
The reaction mixture is then cooled to 20 ° C and the system is added methanol 880 - ammonium hydroxide (2: 1) 600 ml temperature is maintained below 50 ° C, the Solvents are then evaporated in a Buch flask with a water pump at 0 ° C for 1 h, then under high vacuum (about 1 m Hg) at 7G ° C for 1 h (total distillate volume about 600 ml) to obtain the syrup residue.
The syrup residue is mixed with pyridine (HL) and acetic anhydride (1 L), added while maintaining the temperature below 60 ° C. When the dissolution is complete, the reaction mixture is refluxed for 2 hours. The reconstituted mixture is cooled to and added with Cl methanol (200 ml), keeping the temperature below. The solution is then evaporated at 7 (fc with a water pump for an hour, followed by evaporation for about 4 hours under high vacuum (5-7 mm Hg) until about 1300 ml of distillate is collected.
The residue is extracted with hot tolu
at 0 ° C for an additional hour, and prepared with d ol (about 60 ° C) (4-1 L). Extraction crystals are filtered into two portions of the mixture with each part being treated with DyF (2-200 No. 1), then diethyl ether (500 ml) Suiat crystals under vacuum B during the night and
: (approximately 1400 g; „
Daph (600 ml) is added to the reagent.
Vilsmeier (approximately 500 i-a-) in a 3-liter flask with a flange on the throat equipped with a stirrer, thermonegrome, a drying bath and an oklazh, a tsani bath, Rast ™ thief ohlak, and; and the mocho acetate sucrose solution from step 2 (containing about 100 g) is added slowlyJ maintaining the procedure below
t / -. o, -, 20 C,
The reaction, stirring the toluene, is concentrated to a syrup (about 160 g), which is dissolved. in ethyl acetate (500 ml). This ethyl acetate solution is washed with water (2 45 300 ml) and the water washes are in turn washed with ethyl acetate (2 "250 ml). The precipitated ethyl acetate extracts are dried over anhydrous sodium sulfate and filtered through charcoal (about 60 g), which is washed with more ethyl acetate (500 ml) “Ethyl acetate solutions are concentrated to a syrup (approximately 130 g, 60-70% THPSA) (1, 4,6-trichloro-pentaacetate galactosucrose)
This syrup is dissolved in hot ethanol (250 ml), which is cooled to room temperature, seeded with crystals.
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the flask is skewed at the oil bash at about 60 ° C and the gas is passed through
Ola (approximately 60 С) (4 1 l). Extraction
toluene is concentrated to a syrup (about 160 g), which is dissolved in ethyl acetate (500 ml). This ethyl acetate solution is washed with water (2 300 ml) and the water washes are in turn washed with ethyl acetate (2 "250 ml). The precipitated ethyl acetate extracts are dried over anhydrous sodium sulfate and filtered through charcoal (about 60 g), which is washed with more ethyl acetate (500 ml ) "Ethyl acetate solutions are concentrated to a syrup (approximately 130 g, 60-70% THPSA) (1, 4,6-trichloro-pentaacetate galactosucrose)
This syrup is dissolved in hot thanol (250 ml), which is cooled to room temperature, seeded with crystals and left to stand.
overnight at room temperature. The resulting crystals are filtered and dried (ca. 50 g, 90% pure). The recrystallization from ethanol is carried out until the pressure drops until the cristapps are 98% pure. (2 or 3 crystallizations are required, the final weight is about 40 grams).
4. Deacetylation
The THPSA crystals (about 40 g) are dissolved in methanol (about 400 ml) in order to obtain a 10% solution. 1 M sodium methoxide was added to pH 9 and the solution was stirred at 4 hours. TLC (- MeOH 4: 1) showed a single large stain corresponding to TGS. Amberlist 15 (a) ion exchange resin was adjusted to pH 7 and the solution was filtered. And concentrated to dryness (25 g). Distilled water (about 250 ml) is added to make a 10% solution, which is filtered through charcoal to obtain a clear, colorless solution. Water is distilled in a Buch flask to form a dry syrup and more water (approximately 9 ml) is added.
for 17 h, then quickly cooled with water and the solvent is evaporated to obtain a residue of 68 g, containing
g approximately 50% sucrose monoacetate. This material is then reacted with Vilsmirer's reagent according to Example 3. The product is deacylated in situ using a methanol solution of sodium methyl sodium 10. The aqueous solution is then extracted with methanol (to remove tetrachloro derivatives) and then with ethyl acetate. The crude TrG is then peracetylized, crystallized as in Example 3.
15 and deacetylate. Crystalline TGS of about 99% purity is obtained
about 5% overall yield.
Thus, the proposed method allows to obtain the target product using a simplified technology and without loss of output.

权利要求:
Claims (3)
[1]
1. The method of obtaining 4, i, 6-trichloro-4,1, 6-tr1-deoxy-galactosucarose (TGS) from sucrose with preliminary protection of individual hydroxyl groups. In the form of acyloxy groups by saddling to obtain 65% by weight / weight 30 of the selective chlorination in 4, D, b - solution. It is agitated and seeded with a carbohydrate-chlorinating agent, crystals. The resulting crystals are filtered, washed quickly with a small volume of cold water and dried under vacuum at a temperature below. 40 C. The weight of the crystals obtained is approximately 10-20 g (these figures are
volume with subsequent deacylation and allocation of the target product, characterized in that
35 simplifying the process for pre-protecting individual hydroxyl groups, sucrose selectively acyl-pyioT in the 6-position with acetic anhydride
35 process simplification to pre-protect individual hydroxyl groups, sucrose selectively acyl-pyioT in the 6-position with acetic anhydride
represent the number of trials and thus yields are given to about 40 g or about 10 to 20 g. Total JQ temperature or at -30 ° С50 С with half pyridine at room temperature -,
sucrose yield is about 7%
Example 4. Sucrose 50 g in pyridine 625 ml, diluted with methyl ethyl ketone (MEK) 400 ml, cooled to -50 ° C and treated with a solution of acetic anhydride 150 ml in MEK 350 ml. The mixture is stirred at -50 ° C
Editor A.Dolinich
by sucrose 6-mrcoacetate or benzoyl halide in dichloromethane in the presence of sodium carbonate at ambient temperature to obtain 45 m of 6-monobenzonone sucrose
[2]
2. The method according to claim 1, characterized in that the sucrose 6-monoacylate before the mercury chlorination step is separated on a cation exchange resin. (
Compiled by I. Fedoseeva Tehred A. Kravchuk Proofreader G. Reshetnik
for 17 h, then quickly cooled with water and the solvent is evaporated to obtain a residue of 68 g, containing
about 50% sucrose monoacetate. This material is then reacted with Vilsmeier's reagent, as in
[3]
3. The product is deacylated on site using a methanol solution of sodium methylate. The aqueous solution is then extruded (digested with methanol (methane) to remove tetrachloro derivatives) and then with ethyl acetate.
and deacetylate. Crystalline TGS of about 99% purity is obtained
about 5% overall yield.
Thus, the proposed method allows to obtain the target product using a simplified technology and without loss of output.
Invention Formula
1. The method of obtaining 4, i, 6-trichloro-4,1, 6-tr1-deoxy-galactosucarose (TGS) from sucrose with preliminary protection of individual hydroxyl groups. - the positions of the carbohydrate-chlorinating agent
chlorination in 4, G, b - positions of carbohydrate-chlorinating agent
volume with subsequent deacylation and allocation of the target product, characterized in that
0 of the selective chlorination in 4, D, b - positions of carbohydrate-chlorinating agent
35 process simplification to pre-protect individual hydroxyl groups, sucrose selectively acyl-pyioT in the 6-position with acetic anhydride
JQ solution or at -30 ° С50 С with half pyridine at room temperature -,

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法律状态:

优先权:

申请号 | 申请日 | 专利标题

GB8022320|1980-07-08|LV920524A| LV5134A3|1980-07-08|1992-12-29|Saturation of 4,1 ', 6'-trichloro-4,1', 6'-trideoxygalactosaccharose|

LTRP674A| LT2148B|1980-07-08|1993-06-22|4,1 ', 6'-TRICHLOR-4,1', 6'-TRIDEOKIGALAKTOSACHAROSE RECEIVING BUDGET|

MD94-0108A| MD125C2|1980-07-08|1994-03-16|Method of obtaining of 4,1', 6'-trichlor-4,1',6'--trideoxygalactozaccharoze|

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