HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → N-[(3-phenoxyphenyl)methylidene]hydroxylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Hydroxylamine HCl | HCID 21645 | — |
| Reactant | 2-(3-Phenoxyphenyl)-1,3-dioxolane | HCID 13643831 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | N-[(3-phenoxyphenyl)methylidene]hydroxylamine | HCID 2393595 | 94% |
Reaction Steps
To a solution of 24.2 g. of 2-(3-phenoxyphenyl)-1,3-dioxolane in 150 ml. of ethyl alcohol a solution of 14 g. of hydroxylammonium chloride in 150 ml. of water is added, and the mixture is boiled until no traces of starting compound can be detected by thin layer chromatography (silica gel, 1:1 mixture of benzene and tetrachloromethane, development: by UV light). Alcohol is distilled off and the aqueous residue is cooled in ice water. The precipitated crystals are filtered off. 20 g. (94%) of 3-phenoxybenzaldehyde oxime are obtained, melting at 45° to 46° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04304938 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-35f5d7ec4b054a5cbd2d738578896b46 |
| Source note | uspto-grants-1981_12 |