HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ethyl 2-t-amyloxycarbonyloxyimino-2-cyanoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl 2-cyano-2-(hydroxyimino)acetate | HCID 6399078 | — |
| Reactant | Carbonochloridic acid, 1,1-dimethylpropyl ester | HCID 15051328 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 2-t-amyloxycarbonyloxyimino-2-cyanoacetate | HCID 54231162 | 39.8% |
Reaction Steps
A solution of t-amyl chloroformate (0.05 mol) in an ether-toluene mixture (30 ml) is cooled to -10°C, and a solution of ethyl 2-hydroxyimino-2-cyanoacetate (7.2 g) and triethylamine (7.0 ml) in dry benzene (50 ml) is dropwise added thereto. The resulting mixture is allowed to stand at room temperature over night. The reaction mixture is admixed with water and filtered. The organic layer is separated, washed with water, dried and concentrated to give ethyl 2-t-amyloxycarbonyloxyimino-2-cyanoacetate (5.1 g) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976635 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-be9f8bf8203142aeaadbd6558865471f |
| Source note | uspto-grants-1976_08 |