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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338093Generated: October 29, 2026

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

https://huagongshe.com/reaction/338093

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 numberUS08889856B2
Source datasetuspto-grants-2014_11
ORD IDord-05236dc1a0c74c3e81e0fae710f08348
Source noteuspto-grants-2014_11