HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Carbamic acid, ethenyl-, methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 87075430 | HCID 87075430 | — |
| Product | Carbamic acid, ethenyl-, methyl ester | HCID 10866270 | — |
| Product | HCID 131718045 | HCID 131718045 | — |
Reaction Steps
U.S. Pat. No. 3,715,385, Wolgemuth, et al. (1973) describes still another method of obtaining N-vinyl carbamic acid esters by condensation-re-arrangement of acrylonitrile carbonate with methanol or ethanol. In Example I, methyl (N-vinyl carbamate) was obtained in 40% yield from carboethoxy acrylohydroxamate at 100° C. using a sodium alkoxy tin catalyst. The carboethoxy acrylohydroxamate is said to decompose at reaction temperature to yield acrylonitrile carbonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05233077 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-a8fada51851e47ac8d15fda088616dfe |
| Source note | uspto-grants-1993_08 |