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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494430Generated: October 25, 2026

2-Chloro-4-fluorophenylacetonitrile → Ammonia

https://huagongshe.com/reaction/494430

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-fluorophenylacetonitrileHCID 2725063—
ReactantSodium borohydrideHCID 4311764—
CatalystDichlorocobalt hexahydrateHCID 517166—
SolventMethanolHCID 887—
ProductAmmoniaHCID 222—
Product2-(2-Chloro-4-fluorophenyl)ethan-1-amineHCID 21888111—

Reaction Steps

Sodium borohydride (1.73 g, 45.51 mmol) was added portionwise to a solution of 2-chloro-4-fluorophenylacetonitrile (1.04 g, 6.15 mmol) and cobalt (II) chloride hexahydrate (2.18 g, 9.22 mmol) in methanol (30 mL) and the mixture was stirred at room temperature for 3 hours. The suspension was then filtered though Celite®, concentrated in vacuo and the residue was partitioned between 1M hydrochloric acid (40 mL) and dichloromethane (40 mL). The aqueous phase was separated, basified to pH 11 with 1M ammonia solution and extracted with dichloromethane (2×40 mL). The combined organic solution was washed with brine (30 mL), dried over magnesium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 98:2:0.2, to afford the title compound as a yellow oil, 350 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07538141B2
Source datasetuspto-grants-2009_05
ORD IDord-11d727eb596642eeb93a3363e9fdedd9
Source noteuspto-grants-2009_05