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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712395Generated: November 4, 2026

Acetic Anhydride → N-[2-(3-fluoro-2-hydroxyphenyl)ethyl]acetamide

https://huagongshe.com/reaction/1712395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantSodium borohydrideHCID 4311764—
Reactant2-(3-Fluoro-2-hydroxyphenyl)acetonitrileHCID 68499413—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMethanolHCID 887—
ProductN-[2-(3-fluoro-2-hydroxyphenyl)ethyl]acetamideHCID 68502069—

Reaction Steps

A solution of 1.54 g of (3-fluoro-2-hydroxyphenyl)acetonitrile, 1.87 ml of acetic anhydride and 2.41 g of nickel chloride hexahydrate in 75 ml of methanol is admixed at 0° C. with 2.72 g of sodium borohydride in portions and stirred at room temperature over 22 hours. The reaction mixture is concentrated by evaporation, and the residue is diluted with ethyl acetate and saturated aqueous sodium bicarbonate solution and clarified by filtration. The aqueous phase is extracted with ethyl acetate (3×). The combined organic phases are dried with sodium sulphate and concentrated by evaporation. The title compound is obtained as a beige solid from the residue by means of flash chromatography (SiO2 60F). Rf=0.23 (95:5 dichloromethane-methanol); Rt=2.60.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790715B2
Source datasetuspto-grants-2010_09
ORD IDord-2c5d81497ccf4f35ac014243d08d01a8
Source noteuspto-grants-2010_09