FI62684C - Foerfarande foer elektrokemisk framstaellning av 2-(2-amino-etyl)-tiofen - Google Patents
Foerfarande foer elektrokemisk framstaellning av 2-(2-amino-etyl)-tiofen Download PDFInfo
- Publication number
- FI62684C FI62684C FI790121A FI790121A FI62684C FI 62684 C FI62684 C FI 62684C FI 790121 A FI790121 A FI 790121A FI 790121 A FI790121 A FI 790121A FI 62684 C FI62684 C FI 62684C
- Authority
- FI
- Finland
- Prior art keywords
- thiophene
- process according
- electrolyte
- organic
- aminoethyl
- Prior art date
Links
- 238000005057 refrigeration Methods 0.000 title 1
- 238000000034 method Methods 0.000 claims description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Natural products CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 11
- UTPOWFFIBWOQRK-ONEGZZNKSA-N 2-[(e)-2-nitroethenyl]thiophene Chemical compound [O-][N+](=O)\C=C\C1=CC=CS1 UTPOWFFIBWOQRK-ONEGZZNKSA-N 0.000 claims description 8
- HVLUYXIJZLDNIS-UHFFFAOYSA-N 2-thiophen-2-ylethanamine Chemical compound NCCC1=CC=CS1 HVLUYXIJZLDNIS-UHFFFAOYSA-N 0.000 claims description 7
- 239000003792 electrolyte Substances 0.000 claims description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 5
- 239000011541 reaction mixture Substances 0.000 claims description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical group ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 4
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 4
- 229910052753 mercury Inorganic materials 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 230000002378 acidificating effect Effects 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- ZOMNIUBKTOKEHS-UHFFFAOYSA-L dimercury dichloride Chemical class Cl[Hg][Hg]Cl ZOMNIUBKTOKEHS-UHFFFAOYSA-L 0.000 claims description 3
- 229910052697 platinum Inorganic materials 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910001514 alkali metal chloride Inorganic materials 0.000 claims description 2
- 229910002804 graphite Inorganic materials 0.000 claims description 2
- 239000010439 graphite Substances 0.000 claims description 2
- 238000006386 neutralization reaction Methods 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- 238000000605 extraction Methods 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 238000005868 electrolysis reaction Methods 0.000 description 3
- 230000005611 electricity Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 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 description 1
- 101100032401 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) pyr-4 gene Proteins 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- PQLVXDKIJBQVDF-UHFFFAOYSA-N acetic acid;hydrate Chemical compound O.CC(O)=O PQLVXDKIJBQVDF-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 239000003146 anticoagulant agent Substances 0.000 description 1
- 230000006502 antiplatelets effects Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000003487 electrochemical reaction Methods 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- DBDCNCCRPKTRSD-UHFFFAOYSA-N thieno[3,2-b]pyridine Chemical class C1=CC=C2SC=CC2=N1 DBDCNCCRPKTRSD-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000000304 vasodilatating effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
- C07D333/20—Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms
-
- 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
- C25B3/25—Reduction
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)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7801992 | 1978-01-25 | ||
| FR7801992A FR2415671A1 (fr) | 1978-01-25 | 1978-01-25 | Procede de preparation d'amino-2 ethyl-2 thiophene par voie electrochimique |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI790121A7 FI790121A7 (fi) | 1979-07-26 |
| FI62684B FI62684B (fi) | 1982-10-29 |
| FI62684C true FI62684C (fi) | 1983-02-10 |
Family
ID=9203795
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI790121A FI62684C (fi) | 1978-01-25 | 1979-01-15 | Foerfarande foer elektrokemisk framstaellning av 2-(2-amino-etyl)-tiofen |
Country Status (19)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5191090A (en) * | 1990-01-25 | 1993-03-02 | Syntex (U.S.A.) Inc. | Preparation of 2-(2'-thienyl)ethylamine derivatives and synthesis of thieno[3,2-c]pyridine derivatives therefrom |
| JP7229710B2 (ja) | 2018-09-26 | 2023-02-28 | 本田技研工業株式会社 | 車両制御装置、車両制御方法、およびプログラム |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2299332A1 (fr) * | 1975-01-31 | 1976-08-27 | Parcor | Procede de preparation de la (thienyl-2)-2-ethylamine et de ses derives |
-
1978
- 1978-01-25 FR FR7801992A patent/FR2415671A1/fr active Granted
- 1978-12-22 GR GR57970A patent/GR65325B/el unknown
-
1979
- 1979-01-04 DE DE7979400005T patent/DE2960070D1/de not_active Expired
- 1979-01-04 EP EP79400005A patent/EP0003446B1/fr not_active Expired
- 1979-01-08 CH CH12079A patent/CH635618A5/fr not_active IP Right Cessation
- 1979-01-09 ES ES476659A patent/ES476659A1/es not_active Expired
- 1979-01-10 LU LU80772A patent/LU80772A1/xx unknown
- 1979-01-12 DK DK013879A patent/DK151904C/da not_active IP Right Cessation
- 1979-01-15 FI FI790121A patent/FI62684C/fi not_active IP Right Cessation
- 1979-01-17 AR AR275192A patent/AR220736A1/es active
- 1979-01-18 AT AT0038379A patent/AT364839B/de not_active IP Right Cessation
- 1979-01-19 PT PT7969105A patent/PT69105A/pt unknown
- 1979-01-23 IT IT47735/79A patent/IT1115135B/it active
- 1979-01-24 NO NO790231A patent/NO151715C/no unknown
- 1979-01-24 GB GB7902545A patent/GB2013196B/en not_active Expired
- 1979-01-24 BE BE0/193053A patent/BE873677A/xx unknown
- 1979-01-24 MX MX797680U patent/MX5460E/es unknown
- 1979-01-25 JP JP54008103A patent/JPS6046190B2/ja not_active Expired
- 1979-01-30 IE IE112/79A patent/IE47783B1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IE47783B1 (en) | 1984-06-13 |
| NO790231L (no) | 1979-07-26 |
| AT364839B (de) | 1981-11-25 |
| FR2415671B1 (enrdf_load_stackoverflow) | 1981-11-20 |
| ATA38379A (de) | 1981-04-15 |
| MX5460E (es) | 1983-08-11 |
| DK151904C (da) | 1988-06-06 |
| DK13879A (da) | 1979-07-26 |
| LU80772A1 (fr) | 1979-05-16 |
| IE790112L (en) | 1979-07-25 |
| IT7947735A0 (it) | 1979-01-23 |
| EP0003446B1 (fr) | 1980-11-26 |
| CH635618A5 (fr) | 1983-04-15 |
| GR65325B (en) | 1980-08-11 |
| EP0003446A1 (fr) | 1979-08-08 |
| GB2013196B (en) | 1982-06-23 |
| IT1115135B (it) | 1986-02-03 |
| FR2415671A1 (fr) | 1979-08-24 |
| PT69105A (fr) | 1979-02-01 |
| JPS54117462A (en) | 1979-09-12 |
| NO151715C (no) | 1985-05-22 |
| ES476659A1 (es) | 1979-05-16 |
| AR220736A1 (es) | 1980-11-28 |
| BE873677A (fr) | 1979-07-24 |
| NO151715B (no) | 1985-02-11 |
| DE2960070D1 (en) | 1981-02-12 |
| JPS6046190B2 (ja) | 1985-10-15 |
| FI62684B (fi) | 1982-10-29 |
| DK151904B (da) | 1988-01-11 |
| FI790121A7 (fi) | 1979-07-26 |
| GB2013196A (en) | 1979-08-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: PARCOR |