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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | tert-Butyl N-allyl-N-[2-oxo-2-(2-thienyl)ethyl]carbamate | HCID 86697895 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl N-allyl-N-[2-hydroxyimino-2-(2-thienyl)ethyl]carbamate | HCID 86697906 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889856B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-05236dc1a0c74c3e81e0fae710f08348 |
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| Source note | uspto-grants-2014_11 |
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