NO318033B1 - Fremgangsmate ved rensing av et aminalkohol - Google Patents
Fremgangsmate ved rensing av et aminalkohol Download PDFInfo
- Publication number
- NO318033B1 NO318033B1 NO19983564A NO983564A NO318033B1 NO 318033 B1 NO318033 B1 NO 318033B1 NO 19983564 A NO19983564 A NO 19983564A NO 983564 A NO983564 A NO 983564A NO 318033 B1 NO318033 B1 NO 318033B1
- Authority
- NO
- Norway
- Prior art keywords
- amino
- propanediol
- butanol
- water
- crystallization
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 41
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims description 16
- 150000001412 amines Chemical class 0.000 title 1
- KJJPLEZQSCZCKE-UHFFFAOYSA-N 2-aminopropane-1,3-diol Chemical compound OCC(N)CO KJJPLEZQSCZCKE-UHFFFAOYSA-N 0.000 claims description 49
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 39
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 claims description 30
- 150000003839 salts Chemical class 0.000 claims description 30
- 238000002425 crystallisation Methods 0.000 claims description 23
- 230000008025 crystallization Effects 0.000 claims description 23
- 239000012458 free base Substances 0.000 claims description 23
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 21
- 239000012535 impurity Substances 0.000 claims description 17
- 239000002904 solvent Substances 0.000 claims description 17
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 16
- 230000007935 neutral effect Effects 0.000 claims description 15
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 14
- 239000000243 solution Substances 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 12
- 238000001556 precipitation Methods 0.000 claims description 11
- 238000010828 elution Methods 0.000 claims description 10
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 10
- 239000003960 organic solvent Substances 0.000 claims description 10
- 239000007864 aqueous solution Substances 0.000 claims description 9
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 claims description 9
- 150000001768 cations Chemical class 0.000 claims description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims description 7
- 150000001450 anions Chemical class 0.000 claims description 7
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 claims description 6
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims description 6
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 5
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 150000002500 ions Chemical class 0.000 claims description 5
- 239000007787 solid Substances 0.000 claims description 5
- 239000004793 Polystyrene Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 229920002223 polystyrene Polymers 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 239000002585 base Substances 0.000 claims description 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical group CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- HPNMFZURTQLUMO-UHFFFAOYSA-O diethylammonium Chemical compound CC[NH2+]CC HPNMFZURTQLUMO-UHFFFAOYSA-O 0.000 claims description 2
- 235000006408 oxalic acid Nutrition 0.000 claims description 2
- 125000000542 sulfonic acid group Chemical group 0.000 claims description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 4
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 2
- DOGCTUGYGZGSFX-UHFFFAOYSA-N 1-aminopropane-1,3-diol Chemical compound NC(O)CCO DOGCTUGYGZGSFX-UHFFFAOYSA-N 0.000 claims 1
- VDGBLRKKPTUYNW-UHFFFAOYSA-N 2-aminopropane-1,3-diol;hydrochloride Chemical compound Cl.OCC(N)CO VDGBLRKKPTUYNW-UHFFFAOYSA-N 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
- 230000001376 precipitating effect Effects 0.000 claims 1
- 239000000047 product Substances 0.000 description 18
- 239000006227 byproduct Substances 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 10
- 238000000746 purification Methods 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- MJFGNVPJJNQWKK-UHFFFAOYSA-N ethyl 5-benzyl-4,6-dihydro-1h-pyrrolo[3,4-c]pyrazole-3-carboxylate Chemical compound C1C=2C(C(=O)OCC)=NNC=2CN1CC1=CC=CC=C1 MJFGNVPJJNQWKK-UHFFFAOYSA-N 0.000 description 5
- KQIGMPWTAHJUMN-UHFFFAOYSA-N 3-aminopropane-1,2-diol Chemical compound NCC(O)CO KQIGMPWTAHJUMN-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000002872 contrast media Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- JEZJSNULLBSYHV-UHFFFAOYSA-N 5-amino-2,4,6-triiodobenzene-1,3-dicarboxylic acid Chemical compound NC1=C(I)C(C(O)=O)=C(I)C(C(O)=O)=C1I JEZJSNULLBSYHV-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 238000004140 cleaning Methods 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 101100412856 Mus musculus Rhod gene Proteins 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229920001429 chelating resin Polymers 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004587 chromatography analysis Methods 0.000 description 2
- 239000012045 crude solution Substances 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000003344 environmental pollutant Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- XQZXYNRDCRIARQ-LURJTMIESA-N iopamidol Chemical compound C[C@H](O)C(=O)NC1=C(I)C(C(=O)NC(CO)CO)=C(I)C(C(=O)NC(CO)CO)=C1I XQZXYNRDCRIARQ-LURJTMIESA-N 0.000 description 2
- 231100000719 pollutant Toxicity 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 238000005292 vacuum distillation Methods 0.000 description 2
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 1
- CHRJZRDFSQHIFI-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;styrene Chemical compound C=CC1=CC=CC=C1.C=CC1=CC=CC=C1C=C CHRJZRDFSQHIFI-UHFFFAOYSA-N 0.000 description 1
- ZGCHLAJIRWDGFE-UHFFFAOYSA-N 1-aminopropane-1,1-diol Chemical class CCC(N)(O)O ZGCHLAJIRWDGFE-UHFFFAOYSA-N 0.000 description 1
- YMFOWIJFFPALOW-UHFFFAOYSA-N 2-(methylamino)propane-1,3-diol Chemical compound CNC(CO)CO YMFOWIJFFPALOW-UHFFFAOYSA-N 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000013475 authorization Methods 0.000 description 1
- KTUQUZJOVNIKNZ-UHFFFAOYSA-N butan-1-ol;hydrate Chemical compound O.CCCCO KTUQUZJOVNIKNZ-UHFFFAOYSA-N 0.000 description 1
- AXCZMVOFGPJBDE-UHFFFAOYSA-L calcium dihydroxide Chemical compound [OH-].[OH-].[Ca+2] AXCZMVOFGPJBDE-UHFFFAOYSA-L 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- QXDMQSPYEZFLGF-UHFFFAOYSA-L calcium oxalate Chemical compound [Ca+2].[O-]C(=O)C([O-])=O QXDMQSPYEZFLGF-UHFFFAOYSA-L 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 229960004647 iopamidol Drugs 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- -1 monoalkyl ether glycols Chemical class 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000003891 oxalate salts Chemical class 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 235000013772 propylene glycol Nutrition 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/02—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/10—Separation; Purification; Stabilisation; Use of additives
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT96MI002546A IT1286523B1 (it) | 1996-12-04 | 1996-12-04 | Processo per la preparazione di un amminoalcol |
| PCT/EP1997/006725 WO1998024755A1 (en) | 1996-12-04 | 1997-12-01 | Process for the purification of an aminoalcohol |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO983564D0 NO983564D0 (no) | 1998-08-03 |
| NO983564L NO983564L (no) | 1998-10-02 |
| NO318033B1 true NO318033B1 (no) | 2005-01-24 |
Family
ID=11375348
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19983564A NO318033B1 (no) | 1996-12-04 | 1998-08-03 | Fremgangsmate ved rensing av et aminalkohol |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5866719A (it) |
| EP (1) | EP0883597B1 (it) |
| JP (1) | JP4190032B2 (it) |
| AU (1) | AU5658098A (it) |
| DE (1) | DE69733410T2 (it) |
| ES (1) | ES2242987T3 (it) |
| IT (1) | IT1286523B1 (it) |
| NO (1) | NO318033B1 (it) |
| PT (1) | PT883597E (it) |
| WO (1) | WO1998024755A1 (it) |
| ZA (1) | ZA9710864B (it) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1317817B1 (it) * | 2000-02-08 | 2003-07-15 | Bracco Spa | Processo per la purificazione di 3-ammino-1,2-propandiolo e2-ammino-1,3-propandiolo, in particolare nella sintesi di mezzi di |
| JP2002220364A (ja) * | 2001-01-30 | 2002-08-09 | Nippon Shokubai Co Ltd | 高純度アルカノールアミンおよびその製造方法 |
| KR101704563B1 (ko) * | 2015-10-12 | 2017-02-08 | 한국화학연구원 | 락타이드 정제공정을 이용한 락타이드 제조방법 및 제조장치 |
| CN109321610B (zh) * | 2018-11-01 | 2022-11-04 | 上海交通大学 | 微生物发酵法高效制备2-氨基-1,3-丙二醇 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4978793A (en) * | 1988-06-23 | 1990-12-18 | W. R. Grace & Co.-Conn. | Novel process for the preparation of serinol |
| US5053545A (en) * | 1988-12-02 | 1991-10-01 | Angus Chemical Company | Method of preparing amino alcohols |
-
1996
- 1996-12-04 IT IT96MI002546A patent/IT1286523B1/it active IP Right Grant
-
1997
- 1997-12-01 DE DE69733410T patent/DE69733410T2/de not_active Expired - Lifetime
- 1997-12-01 ES ES97952845T patent/ES2242987T3/es not_active Expired - Lifetime
- 1997-12-01 EP EP97952845A patent/EP0883597B1/en not_active Expired - Lifetime
- 1997-12-01 AU AU56580/98A patent/AU5658098A/en not_active Abandoned
- 1997-12-01 WO PCT/EP1997/006725 patent/WO1998024755A1/en active IP Right Grant
- 1997-12-01 JP JP51014898A patent/JP4190032B2/ja not_active Expired - Lifetime
- 1997-12-01 PT PT97952845T patent/PT883597E/pt unknown
- 1997-12-03 US US08/984,086 patent/US5866719A/en not_active Expired - Lifetime
- 1997-12-03 ZA ZA9710864A patent/ZA9710864B/xx unknown
-
1998
- 1998-08-03 NO NO19983564A patent/NO318033B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| ITMI962546A1 (it) | 1998-06-04 |
| EP0883597B1 (en) | 2005-06-01 |
| EP0883597A1 (en) | 1998-12-16 |
| JP4190032B2 (ja) | 2008-12-03 |
| DE69733410T2 (de) | 2006-04-27 |
| ITMI962546A0 (it) | 1996-12-04 |
| DE69733410D1 (de) | 2005-07-07 |
| IT1286523B1 (it) | 1998-07-15 |
| US5866719A (en) | 1999-02-02 |
| JP2000505807A (ja) | 2000-05-16 |
| ES2242987T3 (es) | 2005-11-16 |
| ZA9710864B (en) | 1998-06-23 |
| AU5658098A (en) | 1998-06-29 |
| NO983564D0 (no) | 1998-08-03 |
| PT883597E (pt) | 2005-08-31 |
| WO1998024755A1 (en) | 1998-06-11 |
| NO983564L (no) | 1998-10-02 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MK1K | Patent expired |