HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-Acetylbenzenesulfonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium 4-acetylbenzenesulphonate | HCID 23668814 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Acetylbenzenesulfonyl chloride | HCID 266418 | — |
Reaction Steps
A suspension of 100 g. of sodium 4-acetylbenzenesulfonate in 225 ml. of dimethylformamide is treated with 31 ml. of thionyl chloride and the mixture is stirred at room temperature for 5 minutes, then poured into 1 l. of ice water. The resulting precipitate of 4-acetylbenzenesulfonyl chloride is collected by filtration and washed with ice water. The still-damp product may be used as such without further purification. However, if purification is desired, the following procedure may be used: The product is dissolved in methylene chloride and the solution is dried and evaporated at reduced pressure. Th residual sulfonyl chloride is crystallized from benzene/hexane; m.p. 83°-85° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101661 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-9f102b3d37824ffc85a7228d6916c444 |
| Source note | uspto-grants-1978_07 |