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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705865Generated: October 26, 2026

Sodium borohydride → 5-(Hydroxymethyl)-2-(3-(trifluoromethyl)phenoxy)benzonitrile

https://huagongshe.com/reaction/705865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantBenzonitrile, 5-formyl-2-[3-(trifluoromethyl)phenoxy]-HCID 86666203—
SolventEthanolHCID 702—
Product5-(Hydroxymethyl)-2-(3-(trifluoromethyl)phenoxy)benzonitrileHCID 6682543689.5%

Reaction Steps

A mixture of 5-formyl-2-{[3-(trifluoromethyl)phenyl]oxy}benzonitrile (1 g, 3.43 mmol) and NaBH4 (0.156 g, 4.12 mmol) in ethanol (20 mL) was stirred at room temperature for 3 h. The reaction was quenched with NH4Cl saturated solution and extracted with EA. The organic layer was separated and concentrated to afford the title compound (0.9 g, 89% yield) as a white solid. LCMS: rt=3.71 min

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-daa31dd830be488caa0b9496f3650b41
Source noteuspto-grants-2015_11