戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 731168作成日:2026年10月26日

Ethyl trimethylsilylacetate → Ethyl 3-(4-fluorophenyl)-3-(4-hydroxyphenyl)-acrylate

https://huagongshe.com/reaction/731168

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl trimethylsilylacetateHCID 77687—
反応物4-Fluoro-4'-hydroxybenzophenoneHCID 117666—
反応物Lithium HexamethyldisilazideHCID 2733832—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 3-(4-fluorophenyl)-3-(4-hydroxyphenyl)-acrylateHCID 68674988—

反応手順

A solution of lithium hexamethyldisilazide (23.1 mL, 1 M in THF) was added to a stirred solution of ethyl (trimethylsilyl)acetate (2.53 mL, 13.9 mmol) in THF (15 mL) in 10 minutes at −78° C. The reaction mixture was further stirred at this temperature for 20 minutes. A solution of (4-fluoro-phenyl)-(4-hydroxy-phenyl)-methanone (2 g, 9.2 mmol) in THF (30 mL) was slowly added to the reaction mixture. The reaction mixture was brought to 0° C. over 5 hours. The reaction mixture was quenched with saturated ammonium chloride solution, extracted into EtOAc and washed with dilute ammonium chloride solution. The organic layer was dried over magnesium sulfate. The solvent was removed under vacuum, and the resulting product was flash chromatographed on silica gel, giving M1.1 as an oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582803B2
出典データセットuspto-grants-2009_09
ORD IDord-c3b17590bdc5410d85a69b887de178d7
出典メモuspto-grants-2009_09