HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647662Generated: November 2, 2026
Potassium Carbonate → 2-(Dimethylaminosulfonyloxy)benzenesulfonamide
https://huagongshe.com/reaction/1647662
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Dimethylsulphamoyl chloride | HCID 83372 | — |
| Reactant | 2-Hydroxybenzene-1-sulfonamide | HCID 637546 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(Dimethylaminosulfonyloxy)benzenesulfonamide | HCID 13473126 | 70.1% |
Reaction Steps
4.0 g (29 mmol) of potassium carbonate were added to a solution of 5.0 g (29 mmol) of 2-hydroxybenzenesulfonamide in 200 ml of acetonitrile at 25° C. Stirring was carried out for 10 minutes, after which 4.1 g (29 mmol) of dimethylaminosulfonyl chloride were added dropwise at 25° C. and stirring was continued for a further 16 hours at this temperature. The volatile constituents were removed under reduced pressure from a water pump, the residue was taken up in ethyl acetate, the solution was dried over Na2SO4 and the solvent was removed under reduced pressure from a water pump. The remaining residue was stirred vigorously for 1 hour with 100 ml of diethyl ether. The crystalline product was filtered off under suction and dried at 40° C. under reduced pressure. 5.7 g of the title compound were obtained in this manner.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05434124 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-d56e87b29d1a4fffa1a3b0a8f1425e99 |
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| Source note | uspto-grants-1995_07 |
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