Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480484Generated: October 30, 2026

3-Bromo-5-(trifluoromethyl)benzoic acid → [3-Bromo-5-(trifluoromethyl)phenyl]methanol

https://huagongshe.com/reaction/1480484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-5-(trifluoromethyl)benzoic acidHCID 11086788—
SolventTetrahydrofuranHCID 8028—
Product[3-Bromo-5-(trifluoromethyl)phenyl]methanolHCID 29919767—

Reaction Steps

To a stirred solution of 3-bromo-5-(trifluoromethyl)benzoic acid (1 g, 3.72 mmol) in THF (5 ml) at −78° C. with stirring under nitrogen was added dropwise over 10 mins borane tetrahydrofuran complex 1M in THF (18.59 ml, 18.59 mmol) and then the reaction mixture was warmed to RT over 20 hours. The reaction mixture was cooled in an ice/water bath and quenched dropwise with MeOH (10 ml) followed by 1M HCl until effervescence ceased. Water was added and stirred at RT for 30 mins. THF was removed under reduced pressure, and the compound extracted into EtOAc. The organic portion was dried over MgSO4, filtered and concentrated under reduced pressure. Purification was carried out by chromatography on silica using 0-50% EtOAc in Hexanes as eluent to afford the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409895B2
Source datasetuspto-grants-2016_08
ORD IDord-2bafdf9c025d4e3bb15e6a9f4c395e29
Source noteuspto-grants-2016_08