Methods for buffer stabilized aqueous deacylation
원문보기
IPC분류정보
국가/구분
United States(US) Patent
등록
국제특허분류(IPC7판)
A23G-003/00
C07H-001/06
출원번호
US-0116758
(2002-04-05)
발명자
/ 주소
Vernon, Nicholas M.
Micinski, Edward
Catani, Steven J.
Navia, Juan L.
출원인 / 주소
Tate &
Lyle Public Limited Company
대리인 / 주소
RatnerPrestia
인용정보
피인용 횟수 :
16인용 특허 :
16
초록▼
The present invention relates to novel methods for stabilizing aqueous deacylation, via use of buffers in the production of sucralose. The present invention provides a process for producing sucralose from an acyl-sucralose compound whereby the acyl-sucralose compound is deacylated in the presence of
The present invention relates to novel methods for stabilizing aqueous deacylation, via use of buffers in the production of sucralose. The present invention provides a process for producing sucralose from an acyl-sucralose compound whereby the acyl-sucralose compound is deacylated in the presence of a buffering agent, which stabilizes the pH of the feed mixture and decreases the accumulation of undesired anhydro compounds. Further, the present invention provides a process whereby the acyl-sucralose compound is deacylated directly either prior to or after removal of the tertiary amide reaction vehicle from the neutralized chlorination feed mixture. An aqueous solution of sucralose including salts and other compounds is produced, from which sucralose is recovered by extraction and purified by crystallization.
대표청구항▼
1. A process for producing sucralose from a feed mixture comprising an acyl-sucralose compound in an aqueous solution, wherein said process comprises:(a) adjusting the pH of said feed mixture to a range of about 8.0 to about 12.0; (b) maintaining said feed mixture at an appropriate temperature for s
1. A process for producing sucralose from a feed mixture comprising an acyl-sucralose compound in an aqueous solution, wherein said process comprises:(a) adjusting the pH of said feed mixture to a range of about 8.0 to about 12.0; (b) maintaining said feed mixture at an appropriate temperature for sufficient time to effect conversion of said acyl-sucralose compound into free sucralose; (c) adding a buffer to said feed mixture in an amount sufficient to stabilize said pH within said range for the duration of said maintaining step; (d) decreasing said pH of said feed mixture to about 4 to about 8; and (e) recovering sucralose from the product of step (d), thereby obtaining a recovered sucralose. 2. The process of claim 1, wherein said pH is about 10.5.3. The process of claim 1 wherein said buffer is selected from the group consisting of amines, amino acids, phenols, inorganic acids, saccharin, xanthine, hydroquinine, and a mixture thereof.4. The process of claim 3, wherein said amines are selected from the group consisting of ammonia, alkylamines RNH2, dialkylamines R1R2NH, trialkylamines R1R2 R3N, wherein R, R1, R2, and R3 are selected from the group consisting of methyl, ethyl, 1-propyl, 2-propyl, butyl, cyclohexyl, benzyl, pyrrolidinyl, and 2-hydroxypyridyl.5. The process of claim 3, wherein said amino acids are selected from the group consisting of glycine, alanine, arginine, dimethylglycine, cysteine, and a mixture thereof.6. The process of claim 3, wherein said phenols are selected from the group consisting of phenol and resorcinol.7. The process of claim 3, wherein said inorganic acid is a carbonate.8. The process of claim 1, wherein said buffer is dimethylamine or a salt of dimethylamine.9. The process of claim 1 wherein said acyl-sucralose compound is a 6-O-acyl-4,1′,6′-trichloro-4,1′,6′-trideoxygalactosucrose compound.10. The process of claim 9, wherein said 6-O-acyl-4,1′,6′-trichloro-4,1′,6′-trideoxygalactosucrose compound is 6-O-acetyl-4,1′,6′-trichloro-4,1′,6′-trideoxygalactosucrose.11. The process of claim 9, wherein said 6-O-acyl-4,1′,6′-trichloro-4,1′,6′-trideoxygalactosucrose compound is 6-O-benzoyl-4,1′,6′-trichloro-4,1′,6′-trideoxygalactosucrose.12. The process of claim 1 wherein said feed mixture is substantially free of a tertiary amide.13. The process of claim 1 wherein said feed mixture is substantially free of dimethylformamide.14. The process of claim 1, wherein said recovered sucralose contains about 20 ppm or less of an organic solvent.15. The process of claim 14, wherein said organic solvent is selected from the group consisting of: methanol, ethanol, methyl acetate, toluene, pyridine, DMF, dichloromethane, chloroform, and a mixture thereof.16. The process of claim 15, wherein said recovered sucralose contains about 7 ppm or less of methanol.17. The process of claim 15, wherein said recovered sucralose contains about 7 ppm or less of ethanol.18. The process of claim 15, wherein said recovered sucralose contains about 10 ppm or less of methyl acetate.19. The process of claim 15, wherein said recovered sucralose contains about 10 ppm or less of toluene.20. The process of claim 15, wherein said recovered sucralose contains about 20 ppm or less of DMF.21. The process of claim 15, wherein said recovered sucralose contains about 10 ppb or less of dichloromethane.22. The process of claim 15, wherein said recovered sucralose contains about 10 ppb or less of chloroform.
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이 특허에 인용된 특허 (16)
Lee Cheang K. (Singapore SGX), 4′-Halo-substituted sucrose derivatives.
Vernon, Nicholas M.; Walkup, Robert E., Process for recovery of organotin esters from reaction mixtures containing the same and re-use of the recovered organotin compounds.
Jenner Michael R. (Pangbourne GB2) Waite David (Reading GB2) Jackson Graham (Reading GB2) Williams John C. (Wokingham GB2), Process for the preparation of 4,1′,6′-trichloro-4,1′,6′-trideoxygalactosucrose.
Navia Juan L. (Athens GA) Walkup Robert E. (Watkinsville GA) Vernon Nicholas M. (Watkinsville GA) Neiditch David S. (Athens GA), Production of sucralose without intermediate isolation of crystalline sucralose-6-ester.
Rathbone Elner B. (Berkshire GB2) Mufti Khizar S. (Berkshire GB2) Khan Riaz A. (Berkshire GB2) Cheetham Peter S. J. (Kent GB2) Hacking Andrew J. (Berkshire GB2) Dordick Jonathan S. (Berkshire GB2), Tetrachlororaffinose and its use in the preparation of sucralose.
Kerr, John; Jansen, Robert; Leinhos, Duane A.; Wiley, Jr., James Edwin; Camborieux, Sebastien; Baiada, Anthony; Walker, Gordon; Maffezzoni, Carlo, Method for the production of sucralose.
Wang, Fei; He, Haibing; Wu, Jinshan; Yang, Xin; Yu, Yongzhu; Fan, Zhisong, Process for the preparation of sucralose by the deacylation of trichlorosucrose-6-ethyl ester.
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