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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358793Generated: November 2, 2026

3,5-Bis(trifluoromethyl)benzaldehyde → 3,5-Bis(trifluoromethyl)benzyl alcohol

https://huagongshe.com/reaction/1358793

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventTolueneHCID 1140—
Product3,5-Bis(trifluoromethyl)benzyl alcoholHCID 12293382.5%

Reaction Steps

37 g of 3,5-bis(trifluoromethyl)benzaldehyde and 4 g of Raney nickel together with 150 ml of toluene were placed in a reaction vessel at room temperature. The vessel was pressurized with 30 bar of hydrogen gas and the mixture was hydrogenated at 50° C. for 7.5 hours while stirring. The mixture was subsequently cooled to room temperature, depressurized and the catalyst was filtered off. The filtrate was evaporated and the crude product obtained in this way was distilled at 17 mbar. 3,5-bis(trifluoro-methyl)benzyl alcohol having a boiling point of 97° C. was obtained in a yield of 31.5 g and a purity of 97.7%. This corresponds to a yield of 82.5% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596906B2
Source datasetuspto-grants-2003_07
ORD IDord-70cebbb2e6ef4da1ab77095b7f46c662
Source noteuspto-grants-2003_07