ES2366063T3 - Procedimiento para la preparación de sucralosa por cloración de azúcar con trifosgeno (btc). - Google Patents
Procedimiento para la preparación de sucralosa por cloración de azúcar con trifosgeno (btc). Download PDFInfo
- Publication number
- ES2366063T3 ES2366063T3 ES07854397T ES07854397T ES2366063T3 ES 2366063 T3 ES2366063 T3 ES 2366063T3 ES 07854397 T ES07854397 T ES 07854397T ES 07854397 T ES07854397 T ES 07854397T ES 2366063 T3 ES2366063 T3 ES 2366063T3
- Authority
- ES
- Spain
- Prior art keywords
- btc
- sucrose
- ester
- chlorination
- sucralose
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000004376 Sucralose Substances 0.000 title claims abstract description 22
- 238000000034 method Methods 0.000 title claims abstract description 21
- BAQAVOSOZGMPRM-QBMZZYIRSA-N sucralose Chemical compound O[C@@H]1[C@@H](O)[C@@H](Cl)[C@@H](CO)O[C@@H]1O[C@@]1(CCl)[C@@H](O)[C@H](O)[C@@H](CCl)O1 BAQAVOSOZGMPRM-QBMZZYIRSA-N 0.000 title claims abstract description 18
- 235000019408 sucralose Nutrition 0.000 title claims abstract description 18
- 238000002360 preparation method Methods 0.000 title claims abstract description 7
- 235000000346 sugar Nutrition 0.000 title description 4
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 title 1
- 239000000460 chlorine Substances 0.000 title 1
- 229910052801 chlorine Inorganic materials 0.000 title 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims abstract description 30
- 238000005660 chlorination reaction Methods 0.000 claims abstract description 25
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims abstract description 23
- QQVDYSUDFZZPSU-UHFFFAOYSA-M chloromethylidene(dimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)=CCl QQVDYSUDFZZPSU-UHFFFAOYSA-M 0.000 claims abstract description 18
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims abstract description 14
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000003960 organic solvent Substances 0.000 claims abstract description 8
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000002904 solvent Substances 0.000 claims abstract description 6
- 239000005720 sucrose Substances 0.000 claims description 25
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 24
- 229930006000 Sucrose Natural products 0.000 claims description 16
- 239000000203 mixture Substances 0.000 claims description 16
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 15
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract description 24
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 abstract description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 6
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 abstract description 3
- 239000000243 solution Substances 0.000 description 15
- 239000011541 reaction mixture Substances 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 5
- 239000003153 chemical reaction reagent Substances 0.000 description 5
- 239000006188 syrup Substances 0.000 description 5
- 235000020357 syrup Nutrition 0.000 description 5
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- 229960000583 acetic acid Drugs 0.000 description 2
- 239000000908 ammonium hydroxide Substances 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000012362 glacial acetic acid Substances 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 150000008163 sugars Chemical class 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- UCPYLLCMEDAXFR-UHFFFAOYSA-N triphosgene Chemical group ClC(Cl)(Cl)OC(=O)OC(Cl)(Cl)Cl UCPYLLCMEDAXFR-UHFFFAOYSA-N 0.000 description 2
- WSEQXVZVJXJVFP-HXUWFJFHSA-N (R)-citalopram Chemical class C1([C@@]2(C3=CC=C(C=C3CO2)C#N)CCCN(C)C)=CC=C(F)C=C1 WSEQXVZVJXJVFP-HXUWFJFHSA-N 0.000 description 1
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
- FACOTAQCKSDLDE-YKEUTPDRSA-N [(2R,3R,4R,5R,6R)-6-[(2R,3S,4S,5S)-2,5-bis(chloromethyl)-3,4-dihydroxyoxolan-2-yl]oxy-3-chloro-4,5-dihydroxyoxan-2-yl]methyl acetate Chemical compound O[C@@H]1[C@@H](O)[C@@H](Cl)[C@@H](COC(=O)C)O[C@@H]1O[C@@]1(CCl)[C@@H](O)[C@H](O)[C@@H](CCl)O1 FACOTAQCKSDLDE-YKEUTPDRSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000006136 alcoholysis reaction Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000007257 deesterification reaction Methods 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 235000003599 food sweetener Nutrition 0.000 description 1
- 239000003456 ion exchange resin Substances 0.000 description 1
- 229920003303 ion-exchange polymer Polymers 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- -1 sucrose ester Chemical class 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H1/00—Processes for the preparation of sugar derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H5/00—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium
- C07H5/02—Compounds containing saccharide radicals in which the hetero bonds to oxygen have been replaced by the same number of hetero bonds to halogen, nitrogen, sulfur, selenium, or tellurium to halogen
-
- C—CHEMISTRY; METALLURGY
- C13—SUGAR INDUSTRY
- C13K—SACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
- C13K5/00—Lactose
-
- C—CHEMISTRY; METALLURGY
- C13—SUGAR INDUSTRY
- C13K—SACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
- C13K7/00—Maltose
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Biotechnology (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Health & Medical Sciences (AREA)
- Saccharide Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Seasonings (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US552789 | 2006-10-25 | ||
| US11/552,789 US8258291B2 (en) | 2006-10-25 | 2006-10-25 | Process for the preparation of sucralose by the chlorination of sugar with triphosgene (BTC) |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2366063T3 true ES2366063T3 (es) | 2011-10-14 |
Family
ID=39325402
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES07854397T Active ES2366063T3 (es) | 2006-10-25 | 2007-10-24 | Procedimiento para la preparación de sucralosa por cloración de azúcar con trifosgeno (btc). |
Country Status (19)
| Country | Link |
|---|---|
| US (1) | US8258291B2 (enExample) |
| EP (1) | EP2094873B1 (enExample) |
| JP (1) | JP2010508285A (enExample) |
| KR (1) | KR20090082422A (enExample) |
| CN (1) | CN101631878A (enExample) |
| AT (1) | ATE515509T1 (enExample) |
| AU (1) | AU2007308947A1 (enExample) |
| BR (1) | BRPI0718178A2 (enExample) |
| CA (1) | CA2667419A1 (enExample) |
| CY (1) | CY1112434T1 (enExample) |
| DK (1) | DK2094873T3 (enExample) |
| ES (1) | ES2366063T3 (enExample) |
| MX (1) | MX2009004355A (enExample) |
| PL (1) | PL2094873T3 (enExample) |
| PT (1) | PT2094873E (enExample) |
| RU (1) | RU2009119515A (enExample) |
| SI (1) | SI2094873T1 (enExample) |
| TW (1) | TW200833706A (enExample) |
| WO (1) | WO2008052076A2 (enExample) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080103295A1 (en) * | 2006-10-25 | 2008-05-01 | David Losan Ho | Process for the preparation of sucrose-6-ester by esterification in the presence of solid superacid catalyst |
| US7862744B2 (en) * | 2008-07-23 | 2011-01-04 | Mamtek International Limited | Methods and systems for preparing materials for sucralose production |
| MX2013005560A (es) | 2010-11-23 | 2013-08-26 | Lexington Pharmaceuticals Lab Llc | Cloracion de baja temperatura de carbohidratos. |
| US8884004B2 (en) | 2011-09-02 | 2014-11-11 | Divi's Laboratories, Ltd. | Process for the preparation of sucralose |
| ES2574261T3 (es) | 2011-10-14 | 2016-06-16 | Lexington Pharmaceuticals Laboratories, Llc | Cloración de carbohidratos y derivados de carbohidratos |
| CN103087116A (zh) * | 2011-11-07 | 2013-05-08 | 常茂生物化学工程股份有限公司 | 三氯蔗糖的制备方法 |
| CN104774227A (zh) * | 2015-04-08 | 2015-07-15 | 常州市牛塘化工厂有限公司 | 一种蔗糖-6-乙酯的氯化方法 |
| JP6946275B2 (ja) * | 2015-05-29 | 2021-10-06 | ラクシュミ・プラサド・アラパルティＬａｋｓｈｍｉ Ｐｒａｓａｄ ＡＬＡＰＡＲＴＨＩ | スガマデクスおよびその中間体の製造方法 |
| CN105153248A (zh) * | 2015-08-28 | 2015-12-16 | 山东康宝生化科技有限公司 | 在固体光气法合成三氯蔗糖6乙酯过程中的温度控制方法 |
| CN105111250A (zh) * | 2015-08-28 | 2015-12-02 | 山东康宝生化科技有限公司 | 一种利用固体光气进行三氯蔗糖6乙酯的制备方法 |
| JP6815932B2 (ja) * | 2017-05-31 | 2021-01-20 | 株式会社トクヤマ | Ｎ−カルバメート保護カルボキシ無水物の製造方法 |
| CN108203452B (zh) * | 2018-01-24 | 2021-04-06 | 山东康宝生化科技有限公司 | 一种合成三氯蔗糖-6-乙酯的方法 |
| CN110950888B (zh) * | 2019-11-11 | 2022-05-20 | 山东省科学院菏泽分院 | 一种Vilsmeier试剂参与的氯噁酮的制备方法 |
Family Cites Families (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3072725A (en) | 1960-11-14 | 1963-01-08 | Du Pont | Preparation of dimethylformamide |
| EP0043649B1 (en) * | 1980-07-08 | 1984-09-12 | TATE & LYLE PUBLIC LIMITED COMPANY | Process for the preparation of 4, 1',6'-trichloro-4,1',6'-trideoxygalactosucrose (tgs) |
| GB8818430D0 (en) | 1988-08-03 | 1988-09-07 | Tate & Lyle Plc | Process |
| US4980463A (en) | 1989-07-18 | 1990-12-25 | Noramco, Inc. | Sucrose-6-ester chlorination |
| JP3002885B2 (ja) | 1989-11-02 | 2000-01-24 | 住友化学工業株式会社 | ジメチルホルムアミドの回収精製法 |
| JP3514495B2 (ja) * | 1992-10-02 | 2004-03-31 | エーザイ株式会社 | ハロゲン化アミノチアジアゾリル酢酸誘導体の製造法 |
| CO4410191A1 (es) | 1994-09-19 | 1997-01-09 | Lilly Co Eli | SINTESIS DE 3-[4-(2-AMINOETOXI)BENZOIL]-2-ARIL-6- HIDROXIBENZO [b] TIOFENOS |
| US5498709A (en) | 1994-10-17 | 1996-03-12 | Mcneil-Ppc, Inc. | Production of sucralose without intermediate isolation of crystalline sucralose-6-ester |
| RU2217435C2 (ru) * | 1998-05-15 | 2003-11-27 | Ростислав Георгиевич Жбанков | Способ получения 4,1'6'-трихлор-4,1',6'-тридезоксигалактосахарозы |
| ATE230738T1 (de) * | 1998-10-20 | 2003-01-15 | Lundbeck & Co As H | Verfahren zur herstellung von citalopram |
| US6998480B2 (en) | 2002-03-08 | 2006-02-14 | Tate & Lyle Public Limited Company | Process for improving sucralose purity and yield |
| CN1176094C (zh) | 2003-05-23 | 2004-11-17 | 广东省食品工业研究所 | 一种三氯蔗糖的合成方法 |
| US20060205936A1 (en) | 2005-03-14 | 2006-09-14 | Sl Laboratories, Llc | Chlorination of Sucrose-6-esters |
| GB2442619B (en) * | 2005-05-04 | 2010-05-26 | Pharmed Medicare Pvt Ltd | Chlorination of sucrose acylates using triphosgene |
| CN101253189A (zh) | 2005-08-30 | 2008-08-27 | 法马德医疗保险私人有限公司 | 基于从反应混合物中直接萃取到有机溶剂中随后蒸除溶剂的纯化三氯半乳蔗糖的方法 |
| JP2009538293A (ja) | 2006-05-23 | 2009-11-05 | ヴイ ビー メディケア プライヴェート リミテッド | トリクロロガラクトスクロース製造のプロセスストリームからのジメチルホルムアミド及び他の溶媒の回収 |
| US20080103295A1 (en) | 2006-10-25 | 2008-05-01 | David Losan Ho | Process for the preparation of sucrose-6-ester by esterification in the presence of solid superacid catalyst |
-
2006
- 2006-10-25 US US11/552,789 patent/US8258291B2/en not_active Expired - Fee Related
-
2007
- 2007-10-19 TW TW096139365A patent/TW200833706A/zh unknown
- 2007-10-24 WO PCT/US2007/082422 patent/WO2008052076A2/en not_active Ceased
- 2007-10-24 MX MX2009004355A patent/MX2009004355A/es not_active Application Discontinuation
- 2007-10-24 BR BRPI0718178-7A2A patent/BRPI0718178A2/pt not_active Application Discontinuation
- 2007-10-24 EP EP07854397A patent/EP2094873B1/en not_active Not-in-force
- 2007-10-24 CN CN200780043677A patent/CN101631878A/zh active Pending
- 2007-10-24 ES ES07854397T patent/ES2366063T3/es active Active
- 2007-10-24 JP JP2009534841A patent/JP2010508285A/ja active Pending
- 2007-10-24 AT AT07854397T patent/ATE515509T1/de active
- 2007-10-24 DK DK07854397.2T patent/DK2094873T3/da active
- 2007-10-24 AU AU2007308947A patent/AU2007308947A1/en not_active Abandoned
- 2007-10-24 CA CA002667419A patent/CA2667419A1/en not_active Abandoned
- 2007-10-24 PT PT07854397T patent/PT2094873E/pt unknown
- 2007-10-24 SI SI200730686T patent/SI2094873T1/sl unknown
- 2007-10-24 PL PL07854397T patent/PL2094873T3/pl unknown
- 2007-10-24 RU RU2009119515/04A patent/RU2009119515A/ru not_active Application Discontinuation
- 2007-10-24 KR KR1020097010474A patent/KR20090082422A/ko not_active Withdrawn
-
2011
- 2011-08-08 CY CY20111100756T patent/CY1112434T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| ATE515509T1 (de) | 2011-07-15 |
| WO2008052076B1 (en) | 2008-09-12 |
| AU2007308947A1 (en) | 2008-05-02 |
| SI2094873T1 (sl) | 2011-12-30 |
| US8258291B2 (en) | 2012-09-04 |
| EP2094873A4 (en) | 2009-11-25 |
| BRPI0718178A2 (pt) | 2013-12-17 |
| JP2010508285A (ja) | 2010-03-18 |
| CN101631878A (zh) | 2010-01-20 |
| KR20090082422A (ko) | 2009-07-30 |
| MX2009004355A (es) | 2009-08-25 |
| US20080103298A1 (en) | 2008-05-01 |
| CA2667419A1 (en) | 2008-05-02 |
| EP2094873B1 (en) | 2011-07-06 |
| PL2094873T3 (pl) | 2011-10-31 |
| DK2094873T3 (da) | 2011-08-15 |
| TW200833706A (en) | 2008-08-16 |
| WO2008052076A3 (en) | 2008-07-17 |
| EP2094873A2 (en) | 2009-09-02 |
| CY1112434T1 (el) | 2015-12-09 |
| WO2008052076A2 (en) | 2008-05-02 |
| PT2094873E (pt) | 2011-08-24 |
| RU2009119515A (ru) | 2010-11-27 |
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