HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexylbenzene → 4-Cyclohexylbenzene-1-sulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexylbenzene | HCID 13229 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Cyclohexylbenzene-1-sulfonyl chloride | HCID 4339442 | — |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
A solution of 10.6 ml of phenylcyclohexane in 100 ml of methylene chloride was added at 5° C. within 30 minutes to 13.8 ml of chlorosulfonic acid. The mixture was stirred at 5° C. for 1 hour, poured into 400 ml of a 20% ammonium chloride solution and extracted twice with 300 ml of methylene chloride each time. The organic phases were combined, dried with magnesium sulphate and the solvent was removed on a rotary evaporator. 13.6 g of 4-cyclohexyl-benzenesulfonyl chloride separated as a reddish oil, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958910 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-fe06b79832ba4211b5f8354192793c54 |
| Source note | uspto-grants-1999_09 |