참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | Borane | HCID 6331 | — |
| 반응물 | 5-(4-Chlorophenyl)-2-(trifluoromethyl)furan-3-carboxylic acid | HCID 2736644 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (5-(4-Chlorophenyl)-2-trifluoromethylfuran-3-yl)methanol | HCID 21986513 | — |
반응 단계
A mixture of 5-(4-chlorophenyl)-2-(trifluoromethyl)furan-3-carboxylic acid (0.30 g) in tetrahydrofuran (10 ml) stirred under a nitrogen atmosphere at 0° C. was treated with a 1M solution of borane in tetrahydrofuran (10.33 ml) and the reaction stirred at room temperature for 2 hours. The reaction was cooled to 0° C.; treated with methanol (4 ml) and after 15 minutes the reaction mixture was evaporated. The residue was purified by SPE (Si cartridge) sequentially using dichloromethane, chloroform and chloroform:ether (9:1) as eluents to give the title compound as a white 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-81de7a46f06246799d69db5e5b4d91bf |
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| 출처 메모 | uspto-grants-2006_08 |
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