HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl chloroformate → 2-Benzyloxycarbonyloxyimino-2-phenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-(Hydroxyimino)-2-phenylacetonitrile | HCID 69998 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Benzyloxycarbonyloxyimino-2-phenylacetonitrile | HCID 54006122 | 62.1% |
Reaction Steps
A solution of benzyl chloroformate (5.1 g.) in ether (40 ml.) was added to a solution of 2-hydroxyimino-2-phenylacetonitrile (4.4 g.) in a mixture of a 1N potassium hydroxide aqueous solution (30 ml.) and dioxane (10 ml.) under ice-cooling, and the mixture was stirred for 1 hour at the same temperature and for 4 hours at room temperature. The ether layer was separated from the reaction mixture and the aqueous layer was further extracted with ether. Both ether layers were combined, washed with water and dried over magnesium sulfate. The solvent was distilled off and to the residue was added n-hexane. The precipitated crystals were collected by filtration to give 2-benzyloxycarbonyloxyimino-2-phenylacetonitrile (5.2 g.), mp 73° to 75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04010178 |
| Source dataset | uspto-grants-1977_03 |
| ORD ID | ord-f63af131f3ad45978fb060695b4bd757 |
| Source note | uspto-grants-1977_03 |