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HRID 345565作成日:2026年10月24日

Diethyl Ether → alpha-(4-Fluorophenyl)-1,2-benzenedimethanol

https://huagongshe.com/ja/reaction/345565

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Sodium HydroxideHCID 14798—
反応物2-(4-Fluorobenzoyl)benzoic acidHCID 82099—
反応物Aluminium lithium hydrideHCID 21226445—
溶媒WaterHCID 962—
生成物alpha-(4-Fluorophenyl)-1,2-benzenedimethanolHCID 14230258—

反応手順

To 1190 parts of 1,1'-oxybisethane were added at once 50 parts of lithium aluminium hydride. Then there was added dropwise a solution of 213.7 parts of 2-(4-fluorobenzoyl)benzoic acid in 875 parts of 1,1'-oxybixethane so that the mixture was kept at reflux temperature. Upon completion, stirring was continued first for 30 minutes at room temperature, then for 2 hours at reflux and further overnight at room temperature. The reaction mixture was cooled to 0° C. and there were added dropwise successively 50 parts of water, 50 parts of a 15% sodium hydroxide solution and 150 parts of water all at 0° C. The reaction mixture was filtered over Hyflo and washed thoroughly with 1,1'-oxybisethane. The organic phase was separated, washed with water, dried, filtered and evaporated. The residue was crystallized from a mixture of benzene and hexane, yielding 170.4 parts of α-(4-fluorophenyl)-1,2-benzenedimethanol; mp. ±75° C. (intermediate 91).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05057525
出典データセットuspto-grants-1991_10
ORD IDord-83002c2fecf54737a80502cb8ef1e28a
出典メモuspto-grants-1991_10