참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Thioglycolate | HCID 12185 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | N-{3-chloro-1-methyl-3-[4-(trifluoromethyl)phenyl]prop-2-enylidene}-N-methylmethanaminium hexafluorophosphate | HCID 86593913 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Ethyl 3-methyl-5-[4-(trifluoromethyl)phenyl]thiophene-2-carboxylate | HCID 15946279 | — |
반응 단계
Sodium hydride (60% dispersion in mineral oil, 0.528 g) was added to dry ethanol (20 ml), N-{3-chloro-1-methyl-3-[4-(trifluoromethyl)phenyl]prop-2-enylidene}-N-methylmethanaminium hexafluorophosphate (intermediate 34, 2.8 g) was added followed by ethyl thioglycolate (0.79 g) and the mixture heated at 110° C. for 2 hours under nitrogen. The cooled mixture was concentrated in vacuo and the residue partitioned between water and diethyl ether. The organic layer was collected, dried over magnesium sulphate and concentrated to give the title compound as a brown solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07091237B2 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-6ea3ca517d7342f6ac2c54fa506a38d2 |
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| 출처 메모 | uspto-grants-2006_08 |
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