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HRID 253204作成日:2026年10月25日
4-(Trifluoromethyl)thiobenzamide → [5-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-4-yl]acetic acid ethyl ester
https://huagongshe.com/reaction/253204
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-(Trifluoromethyl)thiobenzamide | HCID 2734823 | — |
| 反応物 | Ethyl 4-bromo-3-oxopentanoate | HCID 12780443 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | [5-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-4-yl]acetic acid ethyl ester | HCID 57986743 | 47.2% |
反応手順
To a solution of 4-trifluoromethyl-benzene-thioamide (1.845 g, 9 mmol) in ethanol (15 mL, 200 proof) add ethyl-4-bromo-3-oxo-pentanoate (2.07 g, 9 mmol). Seal this solution warm the solution to 170° C. in a Personal Chemistry™ microwave oven and stir at this temperature for 20 min. Cool the resulting solution to room temperature, concentrate under reduced pressure and purify the residue by flash chromatography (elute with 30% ethyl acetate/10% dichloromethane in heptane) and obtain the title compound as a white solid (1.4 g). MS (ESI) m/z 330 (M+H); H1 NMR (CDCl3) δ1.87 (bs, 1H), 2.49 (s, 3H), 4.86 (s, 2H), 7.67 (d, J=8 Hz, 2H), 8.02 (d, J=8 Hz, 2H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07872032B2 |
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| 出典データセット | uspto-grants-2011_01 |
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| ORD ID | ord-b0bd6ebe0ead4b828c3e19bf2a6e5885 |
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| 出典メモ | uspto-grants-2011_01 |
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