Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338090Generated: October 29, 2026

Hydroxyamine hydrochloride → tert-Butyl N-allyl-N-[2-hydroxyimino-2-phenyl-ethyl]carbamate

https://huagongshe.com/reaction/338090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
Reactanttert-Butyl N-allyl-N-phenacyl-carbamateHCID 86697893—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Producttert-Butyl N-allyl-N-[2-hydroxyimino-2-phenyl-ethyl]carbamateHCID 86697903—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of tert-butyl N-allyl-N-phenacyl-carbamate (3.2 g, 11.6 mmol), hydroxylamine hydrochloride (1.2 g, 17.4 mmol) and sodium acetate (1.4 g, 17.4 mmol) in ethanol (46 mL) is stirred at 70° C. for 18 hours. The reaction is cooled, diluted with water and extracted with dichloromethane. The organic layers are combined, dried over sodium sulfate, filtered, and concentrated under reduced pressure to give the title compound as a mixture of E and Z isomers which is used without further purification (3.16 g, 94%). ES/MS (m/e): 191 (M+H-100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889856B2
Source datasetuspto-grants-2014_11
ORD IDord-00994f3fa7044d94b2cf42d6c74d66cc
Source noteuspto-grants-2014_11