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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622568Generated: October 25, 2026

4-(Trifluoromethyl)benzhydrol → 4-(Trifluoromethyl)benzophenone

https://huagongshe.com/reaction/1622568

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzhydrolHCID 258897—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product4-(Trifluoromethyl)benzophenoneHCID 69767—

Reaction Steps

A solution of 4-(trifluoromethyl)benzhydrol (1.836 g, 7.3 mmol) in anhydrous DCM (65 mL) was treated with manganese(IV) oxide (<5 micron, activated) (5.7 g, 66 mmol). The resulting suspension was stirred at rt for 12 days. The catalyst was removed by filtration through a Celite® brand filter agent pad. The filtrate was concentrated, and the resulting solid was dried under high vacuum to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778941B2
Source datasetuspto-grants-2014_07
ORD IDord-9cb6e0d07be5439e89dbfee072d9e683
Source noteuspto-grants-2014_07