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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470217Generated: November 2, 2026

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

https://huagongshe.com/reaction/470217

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 numberUS08629270B2
Source datasetuspto-grants-2014_01
ORD IDord-d4dfbcd889ca451484dc5a3fdcdf7286
Source noteuspto-grants-2014_01