HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → 2(3H)-Furanone, 5-(2,2-dichloroethenyl)dihydro-4,4-dimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Di-tert-butyl peroxide | HCID 8033 | — |
| Reactant | 3,3-dimethylpent-4-enoic aicd N,N-dimethylamide | HCID 13020109 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2(3H)-Furanone, 5-(2,2-dichloroethenyl)dihydro-4,4-dimethyl- | HCID 10198203 | 380% |
Reaction Steps
A mixture of 40 g (0.26 mole) of 3,3-dimethylpent-4-enoic aicd N,N-dimethylamide, 231 g (1.5 moles) of carbon tetrachloride and 7 g (0.05 mole) of di-tert.-butyl peroxide is stirred for 6 hours at 140° C. in a stainless steel autoclave. 180 g (1.17 mole) of carbon tetrachloride are then distilled from the reaction mixture under reduced pressure, and the residue is stirred with 200 g of water for 1 hour at 80°-90° C. Extraction with methylene chloride, and subsequent distillation of the methylene chloride solution, gives 39 g (0.19 mole) of 5-(2,2-dichlorovinyl)-4,4-dimethyltetrahydrofuran-2-one, of boiling point 101° C./0.27 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04324725 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-13dd550ce60545d794564bec7af82ec6 |
| Source note | uspto-grants-1982_04 |