HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618993Generated: October 30, 2026
Hydroxyamine hydrochloride → tert-Butyl N-allyl-N-[2-hydroxyimino-2-phenyl-ethyl]carbamate
https://huagongshe.com/reaction/1618993
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | tert-Butyl N-allyl-N-phenacyl-carbamate | HCID 86697893 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | tert-Butyl N-allyl-N-[2-hydroxyimino-2-phenyl-ethyl]carbamate | HCID 86697903 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08772282B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-39fce4feccf94ce8adc6bc0c545719bb |
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| Source note | uspto-grants-2014_07 |
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