GB1507920A - Electrochemical manufacture of aromatic and heterocyclic esters - Google Patents
Electrochemical manufacture of aromatic and heterocyclic estersInfo
- Publication number
- GB1507920A GB1507920A GB30186/75A GB3018675A GB1507920A GB 1507920 A GB1507920 A GB 1507920A GB 30186/75 A GB30186/75 A GB 30186/75A GB 3018675 A GB3018675 A GB 3018675A GB 1507920 A GB1507920 A GB 1507920A
- Authority
- GB
- United Kingdom
- Prior art keywords
- aromatic
- acetate
- alkyl
- propionate
- salt
- 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
- 125000003118 aryl group Chemical group 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 title 1
- 239000002253 acid Substances 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 abstract 3
- 150000001491 aromatic compounds Chemical class 0.000 abstract 3
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 abstract 2
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 abstract 2
- 229910002804 graphite Inorganic materials 0.000 abstract 2
- 239000010439 graphite Substances 0.000 abstract 2
- -1 heterocyclic ester Chemical class 0.000 abstract 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 abstract 2
- 229910000831 Steel Inorganic materials 0.000 abstract 1
- XBDYBAVJXHJMNQ-UHFFFAOYSA-N Tetrahydroanthracene Natural products C1=CC=C2C=C(CCCC3)C3=CC2=C1 XBDYBAVJXHJMNQ-UHFFFAOYSA-N 0.000 abstract 1
- HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 125000004423 acyloxy group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 239000006184 cosolvent Substances 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- UEHUZQKLOWYOMO-UHFFFAOYSA-N diethylazanium;acetate Chemical compound CC(O)=O.CCNCC UEHUZQKLOWYOMO-UHFFFAOYSA-N 0.000 abstract 1
- MRQFCJJRLCSCFG-UHFFFAOYSA-N dimethylazanium;formate Chemical compound C[NH2+]C.[O-]C=O MRQFCJJRLCSCFG-UHFFFAOYSA-N 0.000 abstract 1
- 238000004821 distillation Methods 0.000 abstract 1
- 238000005868 electrolysis reaction Methods 0.000 abstract 1
- 239000003792 electrolyte Substances 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 1
- 239000011133 lead Substances 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 abstract 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 abstract 1
- 125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 239000010959 steel Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 abstract 1
- ZAMCTDDIJFNXOH-UHFFFAOYSA-N tributylazanium;acetate Chemical compound CC(O)=O.CCCCN(CCCC)CCCC ZAMCTDDIJFNXOH-UHFFFAOYSA-N 0.000 abstract 1
- PTMFUWGXPRYYMC-UHFFFAOYSA-N triethylazanium;formate Chemical compound OC=O.CCN(CC)CC PTMFUWGXPRYYMC-UHFFFAOYSA-N 0.000 abstract 1
- UPVCRZBVVOXMDA-UHFFFAOYSA-N trimethylazanium;formate Chemical compound OC=O.CN(C)C UPVCRZBVVOXMDA-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
- C25B3/23—Oxidation
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)
- Quinoline Compounds (AREA)
- Furan Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19742434845 DE2434845C3 (de) | 1974-07-19 | Elektrochemische Herstellung aromatischer oder aromatisch-heterocyclischer Alkansäureester |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1507920A true GB1507920A (en) | 1978-04-19 |
Family
ID=5921030
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB30186/75A Expired GB1507920A (en) | 1974-07-19 | 1975-07-18 | Electrochemical manufacture of aromatic and heterocyclic esters |
Country Status (16)
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4024032A (en) * | 1975-03-31 | 1977-05-17 | Hooker Chemicals & Plastics Corporation | Electrochemical acyloxylation of certain aromatic compounds |
| US4089757A (en) * | 1976-12-20 | 1978-05-16 | Uop Inc. | Electrochemical oxidation of alkoxy-substituted aromatic compounds |
| US4096052A (en) * | 1977-03-07 | 1978-06-20 | Hooker Chemicals & Plastics Corp. | Electrochemical hydroxylation of certain aromatic compounds |
| JPS60100690A (ja) * | 1983-11-02 | 1985-06-04 | Tama Kagaku Kogyo Kk | 水酸化第四アンモニウムの製造方法 |
| DE3913166A1 (de) * | 1989-04-21 | 1990-10-25 | Basf Ag | Verfahren zur herstellung von benzaldehyddialkylacetalen und neue benzaldehyddialkylacetale und benzylester |
| CN107460497B (zh) * | 2017-07-07 | 2019-02-26 | 北京工业大学 | 酰基取代的缺电子含氮杂环化合物的电化学催化合成方法 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3252877A (en) * | 1963-12-12 | 1966-05-24 | Socony Mobil Oil Co Inc | Electrochemical preparation of acyloxy derivatives of condensed ring aromatic compounds |
| DE1643693B2 (de) * | 1967-11-11 | 1976-09-09 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von sebacinsaeuredimethylester durch elektrolytische kondensation von adipinsaeuremonomethylester |
-
1975
- 1975-06-16 JP JP50072111A patent/JPS51125034A/ja active Granted
- 1975-06-17 CA CA229,506A patent/CA1056763A/en not_active Expired
- 1975-06-17 IL IL47504A patent/IL47504A/xx unknown
- 1975-06-18 US US05/587,919 patent/US4011145A/en not_active Expired - Lifetime
- 1975-07-04 NO NO752427A patent/NO142449C/no unknown
- 1975-07-16 CH CH931275A patent/CH597368A5/xx not_active IP Right Cessation
- 1975-07-17 HU HU75BA3303A patent/HU173801B/hu unknown
- 1975-07-17 BE BE158398A patent/BE831480A/xx unknown
- 1975-07-17 DD DD187344A patent/DD118606A5/xx unknown
- 1975-07-17 SU SU752155218A patent/SU612620A3/ru active
- 1975-07-17 NL NL7508580A patent/NL7508580A/xx active Search and Examination
- 1975-07-17 FR FR7522380A patent/FR2278797A1/fr active Granted
- 1975-07-18 CS CS755113A patent/CS188230B2/cs unknown
- 1975-07-18 IT IT25566/75A patent/IT1039949B/it active
- 1975-07-18 GB GB30186/75A patent/GB1507920A/en not_active Expired
- 1975-07-18 ZA ZA00754625A patent/ZA754625B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| DE2434845A1 (de) | 1976-02-05 |
| NL7508580A (nl) | 1976-01-21 |
| IL47504A0 (en) | 1975-08-31 |
| CH597368A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1978-03-31 |
| NO142449C (no) | 1980-08-20 |
| ZA754625B (en) | 1976-07-28 |
| NO752427L (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-01-20 |
| DE2434845B2 (de) | 1976-07-22 |
| HU173801B (hu) | 1979-08-28 |
| IL47504A (en) | 1978-06-15 |
| BE831480A (fr) | 1976-01-19 |
| CA1056763A (en) | 1979-06-19 |
| JPS5760429B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1982-12-20 |
| IT1039949B (it) | 1979-12-10 |
| CS188230B2 (en) | 1979-02-28 |
| JPS51125034A (en) | 1976-11-01 |
| FR2278797A1 (fr) | 1976-02-13 |
| FR2278797B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1978-10-13 |
| US4011145A (en) | 1977-03-08 |
| NO142449B (no) | 1980-05-12 |
| AU8232875A (en) | 1976-12-23 |
| DD118606A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-03-12 |
| SU612620A3 (ru) | 1978-06-25 |
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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 |
Effective date: 19920718 |