KR830010045A - β-클로로 아라닌의 제조방법 - Google Patents
β-클로로 아라닌의 제조방법 Download PDFInfo
- Publication number
- KR830010045A KR830010045A KR1019820002154A KR820002154A KR830010045A KR 830010045 A KR830010045 A KR 830010045A KR 1019820002154 A KR1019820002154 A KR 1019820002154A KR 820002154 A KR820002154 A KR 820002154A KR 830010045 A KR830010045 A KR 830010045A
- Authority
- KR
- South Korea
- Prior art keywords
- aziridine
- producing
- carboxylic acid
- chloroalanine
- chloro
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims 3
- 238000004519 manufacturing process Methods 0.000 claims 10
- ASBJGPTTYPEMLP-UHFFFAOYSA-N 3-chloroalanine Chemical compound ClCC(N)C(O)=O ASBJGPTTYPEMLP-UHFFFAOYSA-N 0.000 claims 8
- WBGBOXYJYPVLQJ-UHFFFAOYSA-N aziridine-2-carboxylic acid Chemical class OC(=O)C1CN1 WBGBOXYJYPVLQJ-UHFFFAOYSA-N 0.000 claims 7
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 6
- 229910000041 hydrogen chloride Inorganic materials 0.000 claims 6
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 claims 6
- -1 alkaline earth metal salt Chemical class 0.000 claims 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 claims 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 2
- 150000001340 alkali metals Chemical group 0.000 claims 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 2
- 150000003863 ammonium salts Chemical class 0.000 claims 2
- 239000012736 aqueous medium Substances 0.000 claims 2
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 claims 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims 1
- VZFRKDUMPVRPSK-UHFFFAOYSA-N [Ca].OC(=O)C1CN1 Chemical compound [Ca].OC(=O)C1CN1 VZFRKDUMPVRPSK-UHFFFAOYSA-N 0.000 claims 1
- UNBYBJUZCIDDHF-UHFFFAOYSA-N [K].OC(=O)C1CN1 Chemical compound [K].OC(=O)C1CN1 UNBYBJUZCIDDHF-UHFFFAOYSA-N 0.000 claims 1
- SNYVWOFAPUATQX-UHFFFAOYSA-N [Mg].OC(=O)C1CN1 Chemical compound [Mg].OC(=O)C1CN1 SNYVWOFAPUATQX-UHFFFAOYSA-N 0.000 claims 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 claims 1
- 229910001860 alkaline earth metal hydroxide Inorganic materials 0.000 claims 1
- 229910021529 ammonia Inorganic materials 0.000 claims 1
- 239000001099 ammonium carbonate Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 229910052808 lithium carbonate Inorganic materials 0.000 claims 1
- 239000002994 raw material Substances 0.000 claims 1
- 238000011084 recovery Methods 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/14—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
- C07C227/18—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/14—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/20—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated the carbon skeleton being further substituted by halogen atoms or by nitro or nitroso groups
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- 아지리딘-2-카르본산염과 염화수소를 반응시켜서 β-클로로아라닌을 제조하는 방법에 있어 그 반응을 아지리딘-2-카르본산염에 대하여 2.0∼5.0 몰비의 염화수소를 사용하여 수성 매체중에서 행하여 얻어진 반응용액으로부터 β-클로로아라닌을 선택적으로 정출시킴을 특징으로 하는 β-클로로아라닌의 제조방법
- 제1항에 있어 아지리딘-2-카르본산염이 아지리딘-2-카르본산의 알카리금속 또는 암모늄염인 β-클로로아라닌의 제조방법.
- 제1항에 있어 아지리딘-2-카르본산염이 아지리딘-2-카르본산의 알카리토류금속염인 β-클로로아라닌의 제조방법.
- 제2항에 있어 염화수소를 아지리딘-2-카르본산의 알카리 금속염 또는 암모늄염에 대하여 2.0∼2.5몰비로 사용하는 β-클로로아라닌의 제조방법.
- 제3항에 있어 염화수소를 아지리딘-2-카르본산의 알카리토류금속염에 대하여 4.0∼5.0몰비로 사용하는 β-클로로아라닌의 제조방법.
- 제1항에 있어 아지리딘-2-카르본산염과 염화수소와의 반응이 0∼100℃에서 행해지는 β-클로로아라닌의 제조방법.
- 제1항에 있어 반응 용액중의 β-클로로아라닌과 α-클로로-β-아라닌의 합계농도로서 a) 아지리딘-2-카르본산리륨을 사용한 경우는 10∼47%중량 b) 아지리딘-2-카르본산나트륨을 사용한 경우는 8∼28중량% c) 아지리딘-2-카르본산칼륨을 사용한 경우는 8∼25중량% d) 아지리딘-2-카르본산마그네슘을 사용한 경우는 10∼41중량% e) 아지리딘-2-카르본산 칼슘을 사용한 경우는 10∼46중량% f) 아지리딘-2-카르본산암모늄을 사용한 경우는 8∼31중량%에 있어 반응 용액으로부터 β-클로로아라닌을 선택적으로 정출시키는 β-클로로아라닌의 제조방법.
- 제1항에 있어 β-클로로아라닌을 -30∼40℃에 있어 정출시키는 β-클로로아라닌의 제조방법.
- 아지리딘-2-카르본산염을 수성매체중 2.0~5.0몰비의 염화수소와 반응시키고 생성한 β-클로로아라닌을 선택적으로 정출시켜서 단리하고, β-클로로아라닌 및 α-클로로-β-아라닌을 함유하는 회수액을 알카리금속 또는 알카리토류금속의 수산화물 또는 암모니아로 처리하고 그리하여 얻어진 아지리딘-2-카르본산염을 원료로하여 순환 사용함을 특징으로 하는 β-클로로아라닌의 제조방법.
- 제8항에 있어 회수액의 처리가 0∼100℃에서 행해지는 β-클로로아라닌의 제조방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP73521 | 1981-05-18 | ||
JP7352181A JPS57188548A (en) | 1981-05-18 | 1981-05-18 | Preparation of beta-chloroalanine |
JP10316581A JPS588049A (ja) | 1981-07-03 | 1981-07-03 | β−クロロアラニンの製造法 |
JP103165 | 1981-07-03 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR830010045A true KR830010045A (ko) | 1983-12-24 |
KR860001900B1 KR860001900B1 (ko) | 1986-10-24 |
Family
ID=26414666
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR8202154A KR860001900B1 (ko) | 1981-05-18 | 1982-05-18 | β-클로로 아라닌의 제조법 |
Country Status (8)
Country | Link |
---|---|
US (1) | US4484003A (ko) |
EP (1) | EP0078853B1 (ko) |
KR (1) | KR860001900B1 (ko) |
CA (1) | CA1183869A (ko) |
DE (1) | DE3267381D1 (ko) |
IT (1) | IT1151407B (ko) |
MX (1) | MX158197A (ko) |
WO (1) | WO1982004043A1 (ko) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HUP0201353A3 (en) * | 2000-02-17 | 2003-01-28 | Kaneka Corp | Processes for preparing optically active amino acid derivatives |
RU2633542C2 (ru) * | 2015-12-11 | 2017-10-13 | Федеральное государственное бюджетное образовательное учреждение высшего образования "Пензенский государственный университет архитектуры и строительства" | СПОСОБ ПОЛУЧЕНИЯ БИОЛОГИЧЕСКИ АКТИВНОГО ВЕЩЕСТВА β-ХЛОР-L-АЛАНИНА |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2449675A1 (fr) * | 1979-02-26 | 1980-09-19 | Wade Tamsir | Procede nouveau pour la preparation d'esters et d'acides aliphatiques a-amines b-aromatiques b-monofluores du type de la fluoro-3 phenylalanine |
CA1111444A (en) * | 1979-06-08 | 1981-10-27 | Kazuo Nakayasu | Process for production of beta-chloroalanine |
FR2471366A1 (fr) * | 1979-12-17 | 1981-06-19 | Wade Tamsir | Procede nouveau pour la preparation d'esters, d'amides, et d'acides aliphatiques a-amines-monofluores tels que la fluoroalanine, l'acide amino-2 fluoro-3 butyrique et leurs esters et amides derives |
-
1982
- 1982-05-17 DE DE8282901437T patent/DE3267381D1/de not_active Expired
- 1982-05-17 WO PCT/JP1982/000174 patent/WO1982004043A1/ja active IP Right Grant
- 1982-05-17 US US06/459,634 patent/US4484003A/en not_active Expired - Fee Related
- 1982-05-17 EP EP82901437A patent/EP0078853B1/en not_active Expired
- 1982-05-17 IT IT21318/82A patent/IT1151407B/it active
- 1982-05-18 MX MX192741A patent/MX158197A/es unknown
- 1982-05-18 KR KR8202154A patent/KR860001900B1/ko active
- 1982-05-18 CA CA000403196A patent/CA1183869A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
KR860001900B1 (ko) | 1986-10-24 |
US4484003A (en) | 1984-11-20 |
EP0078853B1 (en) | 1985-11-13 |
IT1151407B (it) | 1986-12-17 |
IT8221318A0 (it) | 1982-05-17 |
EP0078853A1 (en) | 1983-05-18 |
WO1982004043A1 (en) | 1982-11-25 |
MX158197A (es) | 1989-01-16 |
CA1183869A (en) | 1985-03-12 |
DE3267381D1 (en) | 1985-12-19 |
EP0078853A4 (en) | 1983-09-26 |
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