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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618986Generated: November 3, 2026

Hydroxyamine hydrochloride → Benzyl N-allyl-N-[2-hydroxyiminoethyl]carbamate

https://huagongshe.com/reaction/1618986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium Acetate TrihydrateHCID 23665404—
ReactantBenzyl allyl(2-oxoethyl)carbamateHCID 57415664—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductBenzyl N-allyl-N-[2-hydroxyiminoethyl]carbamateHCID 7407441490.3%

Reaction Steps

A solution of benzyl N-allyl-N-(2-oxoethyl)carbamate (25 g, 107 mmol) in acetonitrile (150 mL) is treated with hydroxylamine hydrochloride (9.68 g, 139 mmol) and a solution of sodium acetate trihydrate (16 g, 117.9 mmol) in water (75 mL). The mixture is stirred at room temperature overnight. The acetonitrile is evaporated and the aqueous solution is extracted with ethyl acetate. The organic layer is separated, dried over magnesium sulfate, and concentrated under vacuum to give the title compound (24 g, 90%). ES/MS (m/e): 249 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772282B2
Source datasetuspto-grants-2014_07
ORD IDord-ec86349239394abdabc8c65f7bef617b
Source noteuspto-grants-2014_07