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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705859Generated: October 30, 2026

Sodium borohydride → 2-(4-Chloro-3-(trifluoromethyl)phenoxy)-5-(hydroxymethyl)benzonitrile

https://huagongshe.com/reaction/705859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantBenzonitrile, 2-[4-chloro-3-(trifluoromethyl)phenoxy]-5-formyl-HCID 86666201—
SolventEthanolHCID 702—
Product2-(4-Chloro-3-(trifluoromethyl)phenoxy)-5-(hydroxymethyl)benzonitrileHCID 6682560889.4%

Reaction Steps

To the solution of 2-{[4-chloro-3-(trifluoromethyl)phenyl]oxy}-5-formylbenzonitrile (1.59 g, 4.88 mmol) in ethanol (45 ml), was added NaBH4 (0.203 g, 5.37 mmol). The solution was stirred at room temperature under nitrogen for 1.5 h. After removing the solvent, the residue was dissolved in DCM, then washed with water twice. The solvent was dried over Na2SO4, concentrated to afford the title compound (1.43 g, 89% yield) as a white solid. LCMS: rt=3.31 min, [M+H+]=328

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174968B2
Source datasetuspto-grants-2015_11
ORD IDord-3cf4a20adf074db4b9b8b520d5aefc8f
Source noteuspto-grants-2015_11