HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2(3H)-Furanone, 5-(2,2-dichloroethenyl)dihydro-4,4-dimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | 3,3-dimethylpent-4-enoic aicd N,N-dimethylamide | HCID 13020109 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Product | 2(3H)-Furanone, 5-(2,2-dichloroethenyl)dihydro-4,4-dimethyl- | HCID 10198203 | — |
Reaction Steps
31 g (0.2 mole) of 3,3-dimethyl-pent-4 -enoic acid, N,N-dimethylamide are added dropwise, in the course of 3 hours, to a solution of 1 g of azo-bis-isobutyronitrile in 308 g (2 moles) of carbon tetrachloride at 75°-80° C. The mixture is stirred for 1.5 hours at 75°-80° C., a further 1 g of azo-bis-isobutyronitrile is added, and the temperature is maintained for a further 2 hours. After distilling off the unconverted starting materials at a bath temperature not exceeding 150° C., a residue is left, and this is stirred with 100 ml of water at 80°-90° C. for 1 hour. 17 g (0.08 mole) of 5-(2,2-dichlorovinyl)-4,4-dimethyl-tetrahydrofuran-2-one are thereby obtained as a water-insoluble phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04324725 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-1475f6d53a004e50a311cbb195e9fe41 |
| Source note | uspto-grants-1982_04 |