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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 73478Generated: October 25, 2026

Benzaldehyde → HCID 12787791, compound

https://huagongshe.com/reaction/73478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
Reactantp-Bromobenzhydryl alcoholHCID 98221—
Reactant1-Benzyl-4-bromobenzeneHCID 236000—
SolventChloroformHCID 6212—
ProductHCID 12787791HCID 1278779186%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08829155B2
Source datasetuspto-grants-2014_09
ORD IDord-7766ab21459b46588f604b233799d610
Source noteuspto-grants-2014_09