SU676160A3 - Способ получени сложных диэфиров сукцинил нтарной кислоты - Google Patents
Способ получени сложных диэфиров сукцинил нтарной кислотыInfo
- Publication number
- SU676160A3 SU676160A3 SU752132125A SU2132125A SU676160A3 SU 676160 A3 SU676160 A3 SU 676160A3 SU 752132125 A SU752132125 A SU 752132125A SU 2132125 A SU2132125 A SU 2132125A SU 676160 A3 SU676160 A3 SU 676160A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- ester
- water
- succinyl
- acid
- succinic acid
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 10
- 239000001384 succinic acid Substances 0.000 title claims description 6
- 150000005690 diesters Chemical class 0.000 title 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 16
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Natural products CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
- -1 ethyl acetate ester Chemical class 0.000 claims description 14
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 12
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims description 10
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 8
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims description 5
- 239000000126 substance Substances 0.000 claims description 5
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- 239000002270 dispersing agent Substances 0.000 claims description 3
- 239000012153 distilled water Substances 0.000 claims description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 claims description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 claims description 2
- 238000003756 stirring Methods 0.000 claims description 2
- 125000002730 succinyl group Chemical group C(CCC(=O)*)(=O)* 0.000 claims description 2
- 239000000243 solution Substances 0.000 claims 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 2
- 150000003863 ammonium salts Chemical class 0.000 claims 2
- 239000001913 cellulose Substances 0.000 claims 2
- 229920002678 cellulose Polymers 0.000 claims 2
- 150000002148 esters Chemical class 0.000 claims 2
- 235000011121 sodium hydroxide Nutrition 0.000 claims 2
- 239000002351 wastewater Substances 0.000 claims 2
- WDJHALXBUFZDSR-UHFFFAOYSA-N Acetoacetic acid Natural products CC(=O)CC(O)=O WDJHALXBUFZDSR-UHFFFAOYSA-N 0.000 claims 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims 1
- 102100035475 Blood vessel epicardial substance Human genes 0.000 claims 1
- DKMROQRQHGEIOW-UHFFFAOYSA-N Diethyl succinate Chemical group CCOC(=O)CCC(=O)OCC DKMROQRQHGEIOW-UHFFFAOYSA-N 0.000 claims 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 claims 1
- 101001094636 Homo sapiens Blood vessel epicardial substance Proteins 0.000 claims 1
- 101000608194 Homo sapiens Pyrin domain-containing protein 1 Proteins 0.000 claims 1
- 101000595404 Homo sapiens Ribonucleases P/MRP protein subunit POP1 Proteins 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
- QOSMNYMQXIVWKY-UHFFFAOYSA-N Propyl levulinate Chemical compound CCCOC(=O)CCC(C)=O QOSMNYMQXIVWKY-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 239000012062 aqueous buffer Substances 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- HFLMYYLFSNEOOT-UHFFFAOYSA-N methyl 4-chloro-3-oxobutanoate Chemical compound COC(=O)CC(=O)CCl HFLMYYLFSNEOOT-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 229910052708 sodium Inorganic materials 0.000 claims 1
- 239000011734 sodium Substances 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 125000004494 ethyl ester group Chemical group 0.000 description 2
- 241000283725 Bos Species 0.000 description 1
- 241001585714 Nola Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- NDKBVBUGCNGSJJ-UHFFFAOYSA-M benzyltrimethylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)CC1=CC=CC=C1 NDKBVBUGCNGSJJ-UHFFFAOYSA-M 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000004714 phosphonium salts Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- BRKFQVAOMSWFDU-UHFFFAOYSA-M tetraphenylphosphanium;bromide Chemical compound [Br-].C1=CC=CC=C1[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 BRKFQVAOMSWFDU-UHFFFAOYSA-M 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C69/757—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/95—Esters of quinone carboxylic acids
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH616674A CH563334A5 (enExample) | 1974-05-07 | 1974-05-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU676160A3 true SU676160A3 (ru) | 1979-07-25 |
Family
ID=4305302
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU752132125A SU676160A3 (ru) | 1974-05-07 | 1975-05-06 | Способ получени сложных диэфиров сукцинил нтарной кислоты |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US4039570A (enExample) |
| JP (1) | JPS50151844A (enExample) |
| AR (1) | AR205122A1 (enExample) |
| AT (1) | AT335996B (enExample) |
| BE (1) | BE828823R (enExample) |
| BG (1) | BG24405A4 (enExample) |
| BR (1) | BR7502748A (enExample) |
| CA (1) | CA1065337A (enExample) |
| CH (1) | CH563334A5 (enExample) |
| CS (1) | CS181293B2 (enExample) |
| DD (1) | DD117445A6 (enExample) |
| DE (1) | DE2518936C2 (enExample) |
| DK (1) | DK142789C (enExample) |
| ES (1) | ES437503A2 (enExample) |
| FR (1) | FR2270231B2 (enExample) |
| GB (1) | GB1444889A (enExample) |
| HU (1) | HU170297B (enExample) |
| IE (1) | IE41042B1 (enExample) |
| IT (1) | IT1046958B (enExample) |
| LU (1) | LU72422A1 (enExample) |
| NL (1) | NL7505404A (enExample) |
| NO (1) | NO751625L (enExample) |
| PL (1) | PL98229B3 (enExample) |
| RO (1) | RO67905A (enExample) |
| SE (1) | SE7505262L (enExample) |
| SU (1) | SU676160A3 (enExample) |
| YU (1) | YU116275A (enExample) |
| ZA (1) | ZA752885B (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4056551A (en) * | 1975-11-17 | 1977-11-01 | Nippon Gohsei Kagaku Kogyo Kabushiki Kaisha | Preparation of succinylsuccinic acid diesters |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3775467A (en) * | 1971-09-10 | 1973-11-27 | Lonza Ag | Process for the production of alkoxy acetoacetic acid esters |
| CH560670A5 (enExample) * | 1972-03-22 | 1975-04-15 | Lonza Ag | |
| CH562774A5 (enExample) * | 1972-04-11 | 1975-06-13 | Lonza Ag |
-
1974
- 1974-05-07 CH CH616674A patent/CH563334A5/xx not_active IP Right Cessation
-
1975
- 1975-01-01 AR AR258679A patent/AR205122A1/es active
- 1975-04-29 DE DE2518936A patent/DE2518936C2/de not_active Expired
- 1975-04-29 GB GB1775175A patent/GB1444889A/en not_active Expired
- 1975-05-02 JP JP50053794A patent/JPS50151844A/ja active Pending
- 1975-05-05 DD DD185833A patent/DD117445A6/xx unknown
- 1975-05-05 IE IE998/75A patent/IE41042B1/xx unknown
- 1975-05-05 BG BG029868A patent/BG24405A4/xx unknown
- 1975-05-05 ZA ZA00752885A patent/ZA752885B/xx unknown
- 1975-05-05 IT IT49432/75A patent/IT1046958B/it active
- 1975-05-05 CS CS7500003114A patent/CS181293B2/cs unknown
- 1975-05-06 NO NO751625A patent/NO751625L/no unknown
- 1975-05-06 YU YU01162/75A patent/YU116275A/xx unknown
- 1975-05-06 CA CA226,362A patent/CA1065337A/en not_active Expired
- 1975-05-06 HU HULO414A patent/HU170297B/hu unknown
- 1975-05-06 DK DK199475A patent/DK142789C/da not_active Application Discontinuation
- 1975-05-06 BR BR3510/75A patent/BR7502748A/pt unknown
- 1975-05-06 PL PL1975180187A patent/PL98229B3/pl unknown
- 1975-05-06 SU SU752132125A patent/SU676160A3/ru active
- 1975-05-06 AT AT346975A patent/AT335996B/de not_active IP Right Cessation
- 1975-05-06 SE SE7505262A patent/SE7505262L/xx unknown
- 1975-05-07 LU LU72422A patent/LU72422A1/xx unknown
- 1975-05-07 NL NL7505404A patent/NL7505404A/xx not_active Application Discontinuation
- 1975-05-07 BE BE156139A patent/BE828823R/xx active
- 1975-05-07 RO RO7582163A patent/RO67905A/ro unknown
- 1975-05-07 ES ES437503A patent/ES437503A2/es not_active Expired
- 1975-05-07 US US05/575,371 patent/US4039570A/en not_active Expired - Lifetime
- 1975-05-07 FR FR7514344A patent/FR2270231B2/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| AR205122A1 (es) | 1976-04-05 |
| NL7505404A (nl) | 1975-11-11 |
| BG24405A4 (en) | 1978-02-10 |
| JPS50151844A (enExample) | 1975-12-06 |
| ATA346975A (de) | 1976-08-15 |
| HU170297B (enExample) | 1977-05-28 |
| IE41042L (en) | 1975-11-07 |
| BE828823R (fr) | 1975-11-07 |
| AU8093075A (en) | 1976-11-11 |
| GB1444889A (en) | 1976-08-04 |
| DK142789C (da) | 1981-08-17 |
| FR2270231A2 (enExample) | 1975-12-05 |
| PL98229B3 (pl) | 1978-04-29 |
| IE41042B1 (en) | 1979-10-10 |
| YU116275A (en) | 1982-02-28 |
| CA1065337A (en) | 1979-10-30 |
| RO67905A (ro) | 1982-02-01 |
| DK142789B (da) | 1981-01-26 |
| LU72422A1 (enExample) | 1976-03-17 |
| AT335996B (de) | 1977-04-12 |
| IT1046958B (it) | 1980-09-10 |
| NO751625L (enExample) | 1975-11-10 |
| SE7505262L (sv) | 1975-11-10 |
| US4039570A (en) | 1977-08-02 |
| DK199475A (da) | 1975-11-08 |
| DE2518936A1 (de) | 1975-11-27 |
| ZA752885B (en) | 1976-04-28 |
| ES437503A2 (es) | 1977-02-01 |
| CH563334A5 (enExample) | 1975-06-30 |
| DE2518936C2 (de) | 1984-09-20 |
| FR2270231B2 (enExample) | 1982-06-04 |
| CS181293B2 (en) | 1978-03-31 |
| BR7502748A (pt) | 1976-03-16 |
| DD117445A6 (enExample) | 1976-01-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3240775A (en) | Preparation of alpha-l-fucosides and l-fucose from fucoidan | |
| CN101861298B (zh) | 甜菜碱的制备方法 | |
| US2288211A (en) | Process for the production of betaalkoxyaldehydes | |
| SU676160A3 (ru) | Способ получени сложных диэфиров сукцинил нтарной кислоты | |
| US2628982A (en) | Bis (trichlormethyl) sulfone | |
| US4483791A (en) | Recovery of fatty acids from tall oil heads | |
| CN108424347A (zh) | 一种2,4-二氯苯氧乙酸的制备方法 | |
| Gilman et al. | The Constitution of DISULFOXIDES1 | |
| US2648710A (en) | Bis-quaternary salts of 1:10-bis-(dialkylamino)-5:6-dithia-decane | |
| Gilman et al. | The Preparation and Chemical Properties of R3PbNa Compounds | |
| JPS6312048B2 (enExample) | ||
| JPS58198460A (ja) | β−メルカプトプロピオン酸の製造法 | |
| US2179978A (en) | Process for the manufacture of levo-ascorbic acid | |
| CN111269121B (zh) | 一种8-氧代-3,7-二甲基-2,6-辛二烯基羧酸酯化合物的纯化方法 | |
| CZ278975B6 (en) | Process for preparing gamma-butyrobetaine | |
| RU2009105820A (ru) | Способ получения триаллилцианурата | |
| CN106699592A (zh) | 一种制备赖诺普利中间体的方法 | |
| US7642371B2 (en) | Process for preparing dialkyl thiodiglycolates | |
| CN112321428A (zh) | 一种r-(+)-2-(4-羟基苯氧基)丙酸乙酯的合成方法 | |
| KR830000147B1 (ko) | 치아졸리딘-4-카복실산 유도체의 제조방법 | |
| US3190906A (en) | Alkane sulfonic acid esters substituted in beta-position by ether groups and their production | |
| EP0140710A2 (en) | Dialkyl sulphosuccinate composition and process for its preparation | |
| SU1341174A1 (ru) | Способ получени 2-замещенных или 2,2-замещенных 1,3-пропандиолов | |
| US3170957A (en) | Process for the production of asymmetrical dialkyl hydrazines | |
| EA016876B1 (ru) | Способ получения дигидрата 3-(2,2,2-триметилгидразиниум) пропионата |