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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904794Generated: October 30, 2026

4-(Trifluoromethyl)benzoyl chloride → 4-(Trifluoromethyl)benzaldehyde

https://huagongshe.com/reaction/904794

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Trifluoromethyl)benzoyl chlorideHCID 67607—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178418416HCID 178418416—
CatalystHCID 178418390HCID 178418390—
SolventTolueneHCID 1140—
Product4-(Trifluoromethyl)benzaldehydeHCID 6799683%

Reaction Steps

In an apparatus as in Example 2, 100 g of 4-trifluoromethylbenzoyl chloride which had been prepared analogously to Example 1 were hydrogenated in the course of 4 hours at 90° C. in 700 ml of dry toluene with the aid of 3.5 g of Pd-carbon (Pd content: 5% by weight); the conversion was 95%. The Pd-carbon catalyst had been exposed, before the hydrogenation, for 30 minutes in toluene at the boil to a mixture containing 50% by volume each of hydrogen and carbon monoxide. By distillation it was possible to obtain 69.2 g of 4-trifluoromethylbenzaldehyde which had a boiling point of 70°-71° C./20 mbars and an nD20 of 1.4639. Yield: 83% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04420433
Source datasetuspto-grants-1983_12
ORD IDord-97914393e7794d0a9de5102e56574059
Source noteuspto-grants-1983_12