Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 23358662 | HCID 23358662 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 23358655 | HCID 23358655 | — |
Reaction Steps
102.8 g (0.865 mol) of thionyl chloride were added to 71.8 g (0.288 mol) of 2-(ethylsulfonyl)benzenesulfonamide in 500 ml of 1,2-dichloroethane in the course of 30 minutes while stirring at from 70° to 80° C., and the refluxed mixture was stirred for 2.5 hours. After the mixture had been cooled to 50° C., 2 ml of pyridine were added and gaseous phosgene was passed into the refluxed mixture in the course of 5 hours while stirring. Evaporating down gave 84.1 g of the title compound, which was taken up directly in 1,2-dichloroethane for storage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05591694 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-487e8eb5ae034fa093c8ab1ec69f93e0 |
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| Source note | uspto-grants-1997_01 |
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