GB1438335A - Production of diesters of dicarboxylic acids by electrochemical condensation of 'onoesters of dicarboxylic acids - Google Patents
Production of diesters of dicarboxylic acids by electrochemical condensation of 'onoesters of dicarboxylic acidsInfo
- Publication number
- GB1438335A GB1438335A GB4620173A GB4620173A GB1438335A GB 1438335 A GB1438335 A GB 1438335A GB 4620173 A GB4620173 A GB 4620173A GB 4620173 A GB4620173 A GB 4620173A GB 1438335 A GB1438335 A GB 1438335A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dicarboxylic acids
- diesters
- ethylhexyl
- monoester
- oct
- 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.)
- Expired
Links
- 150000001991 dicarboxylic acids Chemical class 0.000 title abstract 3
- 230000005494 condensation Effects 0.000 title abstract 2
- 238000009833 condensation Methods 0.000 title abstract 2
- 150000005690 diesters Chemical class 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 abstract 2
- -1 Dicarboxylic acid diesters Chemical class 0.000 abstract 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 abstract 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 abstract 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 abstract 2
- 150000007514 bases Chemical class 0.000 abstract 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 2
- MBGYSHXGENGTBP-UHFFFAOYSA-N 6-(2-ethylhexoxy)-6-oxohexanoic acid Chemical compound CCCCC(CC)COC(=O)CCCCC(O)=O MBGYSHXGENGTBP-UHFFFAOYSA-N 0.000 abstract 1
- 101100188552 Arabidopsis thaliana OCT3 gene Proteins 0.000 abstract 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 1
- 239000001361 adipic acid Substances 0.000 abstract 1
- 235000011037 adipic acid Nutrition 0.000 abstract 1
- 150000001279 adipic acids Chemical class 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000002704 decyl group Chemical group [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])* 0.000 abstract 1
- VJHINFRRDQUWOJ-UHFFFAOYSA-N dioctyl sebacate Chemical compound CCCCC(CC)COC(=O)CCCCCCCCC(=O)OCC(CC)CCCC VJHINFRRDQUWOJ-UHFFFAOYSA-N 0.000 abstract 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 abstract 1
- 238000005868 electrolysis reaction Methods 0.000 abstract 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 abstract 1
- 150000002311 glutaric acids Chemical class 0.000 abstract 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 1
- REOJLIXKJWXUGB-UHFFFAOYSA-N mofebutazone Chemical group O=C1C(CCCC)C(=O)NN1C1=CC=CC=C1 REOJLIXKJWXUGB-UHFFFAOYSA-N 0.000 abstract 1
- 238000006386 neutralization reaction Methods 0.000 abstract 1
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 abstract 1
- 125000002347 octyl 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])[H] 0.000 abstract 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 abstract 1
- 150000003047 pimelic acids Chemical class 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- 150000003330 sebacic acids Chemical class 0.000 abstract 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 229910000029 sodium carbonate Inorganic materials 0.000 abstract 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Substances [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract 1
- TYFQFVWCELRYAO-UHFFFAOYSA-L suberate(2-) Chemical compound [O-]C(=O)CCCCCCC([O-])=O TYFQFVWCELRYAO-UHFFFAOYSA-L 0.000 abstract 1
- 150000003442 suberic acids Chemical class 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B3/00—Electrolytic production of organic compounds
- C25B3/20—Processes
- C25B3/29—Coupling reactions
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19722248562 DE2248562A1 (de) | 1972-10-04 | 1972-10-04 | Verfahren zur herstellung von dicarbonsaeurediestern durch elektrochemische kondensation von dicarbonsaeuremonoestern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1438335A true GB1438335A (en) | 1976-06-03 |
Family
ID=5858111
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4620173A Expired GB1438335A (en) | 1972-10-04 | 1973-10-03 | Production of diesters of dicarboxylic acids by electrochemical condensation of 'onoesters of dicarboxylic acids |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US3879271A (enrdf_load_stackoverflow) |
| JP (1) | JPS4975518A (enrdf_load_stackoverflow) |
| BE (1) | BE805251A (enrdf_load_stackoverflow) |
| CA (1) | CA1029329A (enrdf_load_stackoverflow) |
| DE (1) | DE2248562A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2202059B1 (enrdf_load_stackoverflow) |
| GB (1) | GB1438335A (enrdf_load_stackoverflow) |
| IT (1) | IT998637B (enrdf_load_stackoverflow) |
| NL (1) | NL7312464A (enrdf_load_stackoverflow) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1081830B (it) * | 1976-06-10 | 1985-05-21 | Battelle Memorial Institute | Procedimento di trasferimento di idrogeno in continuo mediante un idruro metallico fra un mezzo liquido acquoso e un composto organico da idrogenare o da deidrogenare |
| US4097344A (en) * | 1976-06-29 | 1978-06-27 | E. I. Du Pont De Nemours And Company | Electrochemical coupling of perfluoroalkyl iodides |
| JPS5422317A (en) * | 1977-07-20 | 1979-02-20 | Asahi Chem Ind Co Ltd | Electrolitic preparation of sebacic acid dimethyl ester |
| DE3276485D1 (en) * | 1982-01-12 | 1987-07-09 | Asahi Chemical Ind | Process for producing higher dibasic acid dimethyl ester |
| ATA134894A (de) * | 1994-07-08 | 1997-12-15 | Hafslund Nycomed Pharma | Verfahren zur herstellung substituierter diaminodicarbonsäurederivate |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL286827A (enrdf_load_stackoverflow) * | 1962-09-17 | |||
| DE1643693B2 (de) * | 1967-11-11 | 1976-09-09 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von sebacinsaeuredimethylester durch elektrolytische kondensation von adipinsaeuremonomethylester |
| US3589990A (en) * | 1968-02-29 | 1971-06-29 | Vnii Pi Monomerov | Process for the production of sebacic acid |
| DE2014985C3 (de) * | 1970-03-28 | 1978-06-08 | Basf Ag, 6700 Ludwigshafen | Verfahren zur elektrolytischen Kondensation von Carbonsäuren |
-
1972
- 1972-10-04 DE DE19722248562 patent/DE2248562A1/de active Pending
-
1973
- 1973-09-10 NL NL7312464A patent/NL7312464A/xx unknown
- 1973-09-19 IT IT29130/73A patent/IT998637B/it active
- 1973-09-25 BE BE135987A patent/BE805251A/xx unknown
- 1973-10-02 FR FR7335135A patent/FR2202059B1/fr not_active Expired
- 1973-10-02 CA CA182,490A patent/CA1029329A/en not_active Expired
- 1973-10-03 GB GB4620173A patent/GB1438335A/en not_active Expired
- 1973-10-03 JP JP48110606A patent/JPS4975518A/ja active Pending
- 1973-10-04 US US403614A patent/US3879271A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| DE2248562A1 (de) | 1974-04-11 |
| IT998637B (it) | 1976-02-20 |
| NL7312464A (enrdf_load_stackoverflow) | 1974-04-08 |
| FR2202059B1 (enrdf_load_stackoverflow) | 1977-08-12 |
| US3879271A (en) | 1975-04-22 |
| FR2202059A1 (enrdf_load_stackoverflow) | 1974-05-03 |
| CA1029329A (en) | 1978-04-11 |
| BE805251A (fr) | 1974-03-25 |
| JPS4975518A (enrdf_load_stackoverflow) | 1974-07-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |