HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → Benzenesulfonyl chloride, 4-chloro-3-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Chlorine monoxide | HCID 24646 | — |
| Reactant | Sulfolane | HCID 31347 | — |
| Reactant | Benzenesulfonic acid, 4-chloro-3-nitro-, potassium salt | HCID 81181 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Benzenesulfonyl chloride, 4-chloro-3-nitro- | HCID 7323 | — |
Reaction Steps
To a mixed solution containing 1,280 g of potassium 4-chloro-3-nitrobenzenesulfonate, 1,150 ml of acetonitrile, 250 ml of Sulfolane (tetrahydrothiophene 1,1-dioxide) and 30 ml of dimethylacetamide was dropwise added 1,250 ml of phoshporus oxychloride under an inside temperature at 60° C. to 70° C. After the reaction was continued for 3 hours at 73° C., the reaction mixture was cooled with water, and thereto was slowly added 400 ml of water. The thus obtained product was poured into 5 liters of ice-cold water. The crystalline precipitate was filtered off, washed with water, and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04916047 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-ec128a30c98840e18b7c5874721e8e87 |
| Source note | uspto-grants-1990_04 |