HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Ethylsulfonyl)ethene → HCID 53685976, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Ethylsulfonyl)ethene | HCID 74680 | — |
| Reactant | 4-Chlorobenzenesulfenylchloride | HCID 11084465 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53685976 | HCID 53685976 | — |
Reaction Steps
4-chlorophenylsulfenyl chloride, 7.5 g was added to 5.0 g of ethyl vinyl sulfone in 20 ml of dichloromethane. There was no exotherm and the system was refluxed for 3 hours. The dichloromethane was removed by stripping and the residue was dissolved in 50 ml of benzene. Triethylamine, 4.2 g, was added dropwise with cooling and after standing for 1 hour, the triethylamine hydrochloride was removed by filtration and the benzene stripped to give a crude product. Purification was carried out by chromatography on a silica gel column. The product, ethyl 2-(4-chlorophenylthio)vinyl sulfone, 4.2 g, was obtained as a clear oil showing one spot by thin-layer chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04196152 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-d56362e8bac64ab3a7ef34fadb521ca6 |
| Source note | uspto-grants-1980_04 |