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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178764Generated: October 30, 2026

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

https://huagongshe.com/reaction/2178764

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 numberUS09067921B2
Source datasetuspto-grants-2015_06
ORD IDord-e69a00be22d5446294a2a0c82a251291
Source noteuspto-grants-2015_06