HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754906Generated: October 28, 2026
Potassium Nitrate → 2-(4-Dimethylcarbamoyl-2-methyl-phenyl)-ethanesulfonyl chloride
https://huagongshe.com/reaction/1754906
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Nitrate | HCID 24434 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 4-(2-mercapto-ethyl)-3,N,N-trimethyl-benzamide | HCID 86672759 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Dimethylcarbamoyl-2-methyl-phenyl)-ethanesulfonyl chloride | HCID 86672760 | 74% |
Reaction Steps
Potassium nitrate (583 mg, 5.77 mmol) was added to a solution of 4-(2-mercapto-ethyl)-3,N,N-trimethyl-benzamide (514 mg, 2.30 mmol) in MeCN (23 ml) at room temperature. The mixture was cooled to −40° C., and sulfuryl chloride (1.68 M solution in dichloromethane, 3.46 ml, 5.81 mmol) was then added dropwise over 15 minutes. After stirring at −40° C. to −20° C. for 2.5 hours, the reaction mixture was diluted with dichloromethane (80 ml) and quenched with a saturated aqueous sodium bicarbonate solution (20 ml). The organic layer and the aqueous layer were separated, and the organic layer was then washed with a saturated aqueous sodium chloride solution (30 ml), dried over MgSO4 and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1→1/2) to give 2-(4-dimethylcarbamoyl-2-methyl-phenyl)-ethanesulfonyl chloride as a colorless solid (491 mg, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169254B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-3a8967aa22264254b5822a79ad3c84ac |
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| Source note | uspto-grants-2015_10 |
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