HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → alpha-[(hydroxyamino)iminomethyl]-N-(2,4,6-trimethoxyphenyl)-benzeneacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | alpha-Cyano-N-(2,4,6-trimethoxyphenyl)benzene acetamide | HCID 10496352 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | alpha-[(hydroxyamino)iminomethyl]-N-(2,4,6-trimethoxyphenyl)-benzeneacetamide | HCID 70113100 | — |
Reaction Steps
Hydroxylamine hydrochloride (11.95 g, 0.17 mol) was added to a solution of triethylamine (23.9 mL, 0.17 mol) in 50% ethanol/water (40 mL), and the mixture was stirred with ice, cooling until the NH2OH.HCl dissolved (0.5 hour). The mixture was then diluted with ethanol (300 mL) and α-cyano-N-(2,4,6-trimethoxyphenyl)-benzene acetamide (44.9 g, 0.138 mol) added in one portion and the mixture refluxed for 8 hours, allowed to cool, and poured into water (2 L) to yield a 2-phase oil/water mixture. The aqueous phase was concentrated in vacuo and the precipitate collected. The oil phase was triturated with chloroform to yield a white solid which was combined with the previous lot to yield 33.6 g, 68%, %(found): C, 60.35; H, 6.11; N, 11.60.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05441975 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-6e68f7cd9b424c12ad68afd3bee16641 |
| Source note | uspto-grants-1995_08 |