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HRID 2368945作成日:2026年10月26日

2,5-Dimethoxybenzoyl chloride → Methyl 3-(2,5-dimethoxyphenyl)-2-(3-methoxy-4-(trifluoromethyl)phenyl)-3-oxopropanoate

https://huagongshe.com/reaction/2368945

反応式

関与物質

役割名称HCID仕込み量
反応物2,5-Dimethoxybenzoyl chlorideHCID 87364—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物Methyl 2-(3-methoxy-4-(trifluoromethyl)phenyl)acetateHCID 86682916—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 3-(2,5-dimethoxyphenyl)-2-(3-methoxy-4-(trifluoromethyl)phenyl)-3-oxopropanoateHCID 8668291797.3%

反応条件

温度-78 °C

反応手順

To a solution of methyl 2-(3-methoxy-4-(trifluoromethyl)phenyl)acetate (18.6 g, 75 mmol) in anhydrous THF (250 mL) at −78° C., LiHMDS (1.0 M in THF, 79 mL, 79 mmol) was added dropwise under N2. The resulting mixture was stirred at −78° C. for 30 minutes, and a solution of 2,5-dimethoxybenzoyl chloride (15.9 g, 78 mmol; intermediate in Intermediate 1) in anhydrous THF (50 mL) was added dropwise. The reaction mixture was stirred for another 1 h at −78° C., quenched with saturated aqueous NH4Cl (100 mL), and extracted with ethyl acetate (2×100 mL). The combined organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum to give the title compound (30.1 g). 1H NMR (DMSO-d6): δ 7.50 (d, 1H), 7.34 (d, 1H), 7.09-7.07 (m, 1H), 6.94-6.87 (m, 3H), 5.71 (s, 1H), 3.92 (s, 3H), 3.85 (s, 3H), 3.77 (s, 3H), 3.65 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08703810B2
出典データセットuspto-grants-2014_04
ORD IDord-d63be15e53e44fd49f152276629b2da4
出典メモuspto-grants-2014_04