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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581105Generated: October 30, 2026

Acetohydroxamic Acid → N-phenylmethoxyacetamide

https://huagongshe.com/reaction/581105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetohydroxamic AcidHCID 1990—
ReactantDimethylformamideHCID 6228—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
SolventWaterHCID 962—
ProductN-phenylmethoxyacetamideHCID 512918465%

Reaction Steps

60% sodium hydride (11.68 g, 0.292 mol) was added to a dimethylformamide solution (200 ml) of acetohydroxamic acid (21.9 g, 0.292 mol) with cooling in an ice bath. After stirring for 1 hour at room temperature, benzylbromide (50 g, 0.292 mol) was added thereto and allowed to react for 24 hours at room temperature. The reaction solution was poured into 500 ml of water, and extracted with ethyl acetate. The organic layer was rinsed with water and dried. After removing the solvent by evaporation, the residue was purified with silica gel chromatography to obtain 31.3 g of N-benzyloxyacetamide (yield: 65%). The proton NMR spectrum of the compound is 1.85 s (3H); 4.89 bs (2H); 7.37 s (5 H); 8.30 bs, 8.81 bs (1H) (solvent: CDCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919825
Source datasetuspto-grants-1999_07
ORD IDord-add983a55a394e76bb629d2827054bd7
Source noteuspto-grants-1999_07