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HRID 1703786作成日:2026年10月25日

Acetaldehyde → 1-(4'-Trifluoromethyl-biphenyl-4-yl)-ethanol

https://huagongshe.com/reaction/1703786

反応式

関与物質

役割名称HCID仕込み量
反応物AcetaldehydeHCID 177—
反応物MagnesiumHCID 5462224—
反応物4-Bromo-4'-(trifluoromethyl)biphenylHCID 12712349—
触媒BromineHCID 24408—
溶媒TetrahydrofuranHCID 8028—
生成物1-(4'-Trifluoromethyl-biphenyl-4-yl)-ethanolHCID 22760332—

反応条件

温度0 °C

反応手順

To a stirred suspension of 1.5 g of magnesium turnings in 10 ml of dry tetrahydrofuran, add a small amount of 4'-trifluoromethyl-4-bromo[1,1']biphenyl and a few drops of bromine. When the reaction is started, add (dropwise) a solution of 16 g of 4'-trifluoromethyl-4-bromo-[1,1']biphenyl in 50 ml of tetrahydrofuran at 50°-60° C. Heat the mixture for one hour, cool to 0° C., and slowly (dropwise) add 7 g of acetaldehyde. Stir the reaction mixture at room temperature for twenty hours. Work-up the reaction mixture following the procedure of example 2, and isolate the desired product by chromatography, m.p. 116°-117°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04125612
出典データセットuspto-grants-1978_11
ORD IDord-fa52e0b551834cedb292336b24ee4b2d
出典メモuspto-grants-1978_11