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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244903Generated: November 2, 2026

Sodium borohydride → 2-Bromo-5-(trifluoromethyl)benzyl alcohol

https://huagongshe.com/reaction/2244903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2-Bromo-5-(trifluoromethyl)benzaldehydeHCID 7018047—
SolventTetrahydrofuranHCID 8028—
Product2-Bromo-5-(trifluoromethyl)benzyl alcoholHCID 275624886.3%

Reaction Steps

To a mixture of 2-bromo-5-(trifluoromethyl)benzaldehyde (5 g, 20 mmol) in THF (20 mL) at 0° C. was added sodium borohydride (0.8 g, 20 mmol). The resulting mixture was stirred at 0° C. to ambient temperature for 1 h. The reaction was quenched by addition of an aqueous solution of NaHCO3. The resulting solution was extracted with EtOAc twice. The combined extracts were washed with brine, dried (MgSO4), filtered and concentrated to give the desired alcohol as a white solid (4.4 g). 1H NMR (CDCl3) δ 7.81 (s, 1H), 7.66 (d, J=8.3 Hz, 1H), 7.42 (dd, J=8.3 Hz, 2.0 Hz, 1H), 4.81 (d, J=6.3 Hz, 2H), 2.03 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678798B2
Source datasetuspto-grants-2010_03
ORD IDord-0f553f19f73240cc91e7d6bfa125b381
Source noteuspto-grants-2010_03