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HRID 73478作成日:2026年10月26日

Benzaldehyde → alpha,alpha'-Diphenyl-alpha-hydroxyl-p-xylene

https://huagongshe.com/reaction/73478

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物p-Bromobenzhydryl alcoholHCID 98221—
反応物1-Benzyl-4-bromobenzeneHCID 236000—
溶媒ChloroformHCID 6212—
生成物alpha,alpha'-Diphenyl-alpha-hydroxyl-p-xyleneHCID 1278779186%

反応手順

α,α′-Diphenyl-α-hydroxyl-p-xylene was prepared as shown in Scheme 4 by using 29.0 g (117 mmol) of 4-bromo diphenylmethane and 11.2 g (106 mmol) of benzaldehyde/19.7 g (106 mmol) by the similar procedure to the method for preparing 4-bromobenzhydrol. The crude product was dissolved in chloroform and filtered through G60 column filled with silica gel. After evaporating the solvent, the result product was recrystallized with hexane/chloroform (9:1 v/v) to provide a yield of 86%. MP: 64° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829155B2
出典データセットuspto-grants-2014_09
ORD IDord-7766ab21459b46588f604b233799d610
出典メモuspto-grants-2014_09