HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-CHLORO-1-(p-t-BUTYLPHENYLSULFONYL)ETHYL PHENYL SULFIDE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1-Tert-butyl-4-(ethenesulfonyl)benzene | HCID 879322 | — |
| Reactant | Benzenesulfenyl chloride | HCID 11008040 | — |
| Product | 2-CHLORO-1-(p-t-BUTYLPHENYLSULFONYL)ETHYL PHENYL SULFIDE | HCID 13044808 | 86% |
Reaction Steps
To a solution of 21.0 g (93.7 moles) of p-t-butylphenyl vinyl sulfone in 100 ml of methylene chloride at 20° C. was added 14.0 ml (17,5 g, 121 mmoles) of benzenesulfenyl chloride. After 75 minutes the initial red color of the solution had changed to orange. In the same time the temperature of the solution rose to 26° C. After three days at 23° C. the solvent was removed by evaporation. The semicrystalline residue was recrystallized from ethyl acetate-pentane (1:2) to give a first crop of 18.3 g (53%), m.p. 104.0°-105.5° C. and subsequent crops of 8.3 and 3.0 g, for a total yield of 86%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04335142 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-1811a6e43aa7448284219a9a5057e657 |
| Source note | uspto-grants-1982_06 |