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HRID 2368936作成日:2026年10月27日

Lithium Hexamethyldisilazide → Ethyl 3-(2-fluoro-3,6-dimethoxyphenyl)-2-(3-methoxyphenyl)-3-oxopropanoate

https://huagongshe.com/reaction/2368936

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物Ethyl 3-methoxyphenylacetateHCID 2774971—
反応物2-Fluoro-3,6-dimethoxybenzoyl chlorideHCID 86682906—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 3-(2-fluoro-3,6-dimethoxyphenyl)-2-(3-methoxyphenyl)-3-oxopropanoateHCID 8668290786.3%

反応条件

温度-78 °C

反応手順

To a mixture of 2-fluoro-3,6-dimethoxybenzoic acid (4.8 g, 24 mmol) in anhydrous dichloromethane (75 mL) at 0° C., SOCl2 (14.2 g, 120 mmol) was slowly added followed by DMF (0.1 mL). The resulting mixture was stirred at room temperature for 2 h and concentrated in vacuo to give 2-fluoro-3,6-dimethoxybenzoyl chloride (5.2 g). To a solution of ethyl 2-(3-methoxyphenyl)acetate (4.7 g, 24 mmol) in anhydrous THF (40 mL) at −78° C., LiHMDS (1.0 M in THF, 36 mL) was added dropwise. The resulting solution was stirred at −78° C. for 30 min and a solution of 2-fluoro-3,6-dimethoxybenzoyl chloride (5.2 g, 24 mmol) in anhydrous THF (60 ml) was added dropwise. The reaction mixture was stirred for additional 2 h at −78° C. and quenched with saturated NH4Cl. The mixture was extracted with ethyl acetate (3×200 mL). The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure to afford the title compound (7.8 g).

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-4219e8c2894f44f18e99f7d9a0fe487f
出典メモuspto-grants-2014_04