Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-(2-hydroxyethyl)-N-(1,1-dimethylethyl)benzenesulfonamide | HCID 13822972 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13822973 | HCID 13822973 | — |
Reaction Steps
The alcohol from Example 1 (33.1 g) and 20 ml of triethylamine were dissolved in 350 ml of dichloromethane, cooled to 0° C., and treated with 11 ml methanesulfonyl chloride. After being stirred at room temperature for about 20 hours, the reaction mixture was diluted with dichloromethane (100 ml) and the organic layer was washed with three 50-ml portions of water and one of brine. Drying and concentration in vacuo gave the crude product which gradually crystallized upon standing. The solid was washed with diethyl ether, filtered, and dried to yield 12.0 g of 2-[2-(methylsulfonyloxy)ethyl]-N-(1,1-dimethylethyl)benzenesulfonamide as a white powder; m.p. 106°-108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04662933 |
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| Source dataset | uspto-grants-1987_05 |
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| ORD ID | ord-596babbebc2d431194fb27bb7f10e09f |
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| Source note | uspto-grants-1987_05 |
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