Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405608Generated: October 30, 2026

3,4,5-Trifluorobenzaldehyde → 3,4,5-Trifluorobenzyl alcohol

https://huagongshe.com/reaction/2405608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrifluorobenzaldehydeHCID 2776954—
Reactantwater NaBH4HCID 131728255—
SolventTetrahydrofuranHCID 8028—
Product3,4,5-Trifluorobenzyl alcoholHCID 277704099.8%

Reaction Steps

To a cooled (−5° C.) solution of 3,4,5-trifluorobenzaldehyde (7.0 g, 43.75 mmol) in a mixture (50 ml, 9:1) of THF and water NaBH4 (1.662 g, 43.75 mmol) was slowly added in portions over a period of 30 min. The reaction mixture was allowed to attain room temperature over a period of 2 h and carefully poured into ice-cold dil HCl (200 ml, IN). The oily layer was extracted into CH2Cl2 (250 ml) and the organic layer washed with water (200 ml), dried (MgSO4) and evaporated. The crude product (7.08 g, quantitative) obtained was taken forward without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08808742B2
Source datasetuspto-grants-2014_08
ORD IDord-5dede1c02293473b8f8e87725e0e791b
Source noteuspto-grants-2014_08