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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350603Generated: October 25, 2026

(2-Amino-4-chlorophenyl)methanol → N-(5-chloro-2-hydoxymethylphenyl)formamide

https://huagongshe.com/reaction/350603

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Amino-4-chlorophenyl)methanolHCID 4134900—
Reactant(Formyloxy)acetonitrileHCID 4205685—
SolventTetrahydrofuranHCID 8028—
ProductN-(5-chloro-2-hydoxymethylphenyl)formamideHCID 12083233—

Reaction Steps

A solution of 5.00 g of (2-amino-4-chlorophenyl)methanol, 2.73 g of cyanomethyl formate and 0.04 g of 4-N,N-dimethylaminopyridine in 50 ml of anhydrous tetrahydrofuran was stirred for 72 hours at 20° C. The solvent was then evaporated in vacuo and the residue was taken up in 50 ml of ethyl acetate. The solution was washed in succession twice with in each case 100 ml of 0.01 N hydrochloric acid and saturated sodium chloride solution, dried over sodium sulfate and then concentrated by evaporation in vacuo. The residue was purified by flash chromatography on silica gel with ethyl acetate/cyclohexane (2/1) as eluent. 1.41 g (24% of theory) of the title compound was thereby obtained in the form of slightly yellowish crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183274B2
Source datasetuspto-grants-2007_02
ORD IDord-80d56597d06c4e7d895c9a203c1b9c88
Source noteuspto-grants-2007_02