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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

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Trifluoromethyl)thiobenzamideHCID 2734823—
反応物Ethyl 4-bromo-3-oxopentanoateHCID 12780443—
溶媒EthanolHCID 702—
生成物[5-Methyl-2-(4-trifluoromethyl-phenyl)-thiazol-4-yl]acetic acid ethyl esterHCID 5798674347.2%

反応条件

温度170 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07872032B2
出典データセットuspto-grants-2011_01
ORD IDord-b0bd6ebe0ead4b828c3e19bf2a6e5885
出典メモuspto-grants-2011_01