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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 470220Generated: October 30, 2026

Hydroxyamine hydrochloride → tert-Butyl N-allyl-N-[2-hydroxyimino-2-(2-thienyl)ethyl]carbamate

https://huagongshe.com/reaction/470220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
Reactanttert-Butyl N-allyl-N-[2-oxo-2-(2-thienyl)ethyl]carbamateHCID 86697895—
SolventEthanolHCID 702—
Producttert-Butyl N-allyl-N-[2-hydroxyimino-2-(2-thienyl)ethyl]carbamateHCID 86697906—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of tert-butyl N-allyl-N-[2-oxo-2-(2-thienyl)ethyl]carbamate (15.2 g, 54.0 mmol), hydroxylamine hydrochloride (5.63 g, 81.0 mmol) and sodium acetate (6.65 g 81.0 mmol) in ethanol (216 mL) is stirred at 70° C. for 18 hours. The reaction is cooled and the solvent removed under reduced pressure. The residue is diluted water (100 mL) and extracted with dichloromethane. The organic layers are combined dried over sodium sulfate, filtered and concentrated under reduced pressure to give the crude title compound as a mixture of E and Z isomers, which is used without further purification (16 g, >98%): ES/MS (m/e): 197 (M+H-100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629270B2
Source datasetuspto-grants-2014_01
ORD IDord-0e06c1bd3fb641a39ab2d5bdf22bc350
Source noteuspto-grants-2014_01