HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxyamine hydrochloride → Benzyl N-allyl-N-[2-hydroxyiminoethyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate Trihydrate | HCID 23665404 | — |
| Reactant | Benzyl allyl(2-oxoethyl)carbamate | HCID 57415664 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Benzyl N-allyl-N-[2-hydroxyiminoethyl]carbamate | HCID 74074414 | 90.3% |
Reaction Steps
A solution of benzyl N-allyl-N-(2-oxoethyl)carbamate (25 g, 107 mmol) in acetonitrile (150 mL) is treated with hydroxylamine hydrochloride (9.68 g, 139 mmol) and a solution of sodium acetate trihydrate (16 g, 117.9 mmol) in water (75 mL). The mixture is stirred at room temperature overnight. The acetonitrile is evaporated and the aqueous solution is extracted with ethyl acetate. The organic layer is separated, dried over magnesium sulfate, and concentrated under vacuum to give the title compound (24 g, 90%). ES/MS (m/e): 249 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841293B1 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-9441995f7e9f438e9ef0b36e51468443 |
| Source note | uspto-grants-2014_09 |