HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorosulfonic acid → p-(2-Acetamidoethyl)benzenesulphonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | N-(2-phenylethyl)acetamide | HCID 70143 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | p-(2-Acetamidoethyl)benzenesulphonyl chloride | HCID 3015782 | — |
Reaction Steps
30.6 ml chlorosulfonic acid were added in one portion to 25.0 g N-phenethyl-acetamide. The reaction mixture was stirred at room temperature for one hour, then 100 ml dichloromethane were added and the reaction mixture was poured on ice water. The organic layer was separated washed twice with 50 ml brine and then dried over MgSO4. The solvent was removed in vacuo to obtain 22.0 g 4-(2-Acetylamino-ethyl)-benzenesulfonyl chloride as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858647B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-6cbc2ff5fa174d6185f6771accdfec30 |
| Source note | uspto-grants-2010_12 |