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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040515Generated: October 27, 2026

Hydrochloric Acid → 3-(Hydroxymethyl)-5-(trifluoromethoxy)benzonitrile

https://huagongshe.com/reaction/2040515

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
Reactant3-Cyano-5-(trifluoromethoxy)benzoyl chlorideHCID 86646992—
SolventTetrahydrofuranHCID 8028—
Product3-(Hydroxymethyl)-5-(trifluoromethoxy)benzonitrileHCID 6684753459.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Cyano-5-(trifluoromethoxy)benzoyl chloride (844 mg, 3.38 mmol) was dissolved in THF (10 mL) and cooled to 0° C. Sodium borohydride (320 mg, 8.45 mmol) was added, followed by methanol (2 mL) and the reaction was stirred for 20 min at 0° C. before it was allowed to warm to room temperature. After 2 h, the reaction mixture was acidified to pH 3 with 1.0 M HCl. The aqueous mixture was extracted with ethyl acetate and the combined extracts were dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (440 mg). LCMS m/z=218.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580841B2
Source datasetuspto-grants-2013_11
ORD IDord-8d9714006805436ba1b6e6a4a9480e66
Source noteuspto-grants-2013_11