HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-But-2-ynyloxy-N-methyl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 4-But-2-ynyloxy-benzenesulfonyl chloride | HCID 11195928 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-But-2-ynyloxy-N-methyl-benzenesulfonamide | HCID 11160783 | 92% |
Reaction Steps
To 22.5 mL (0.045 mol) of a 2M solution of methylamine in dichloromethane, cooled to 0° C., was added a solution of 3.67 g (0.015 mol) of 4-but-2-ynyloxy-benzenesulfonyl chloride in 45 mL of dichloromethane. The reaction was allowed to warm to room temperature and stirred for 48 h. The resulting solution was poured into water and extracted with dichloromethane. The combined organics were washed with 2N citric acid solution, water and brine, dried over Na2SO4, filtered through Magnesol® and concentrated in vacuo to provide 3.23 g (92%) of the N-methyl sulfonamide as a white solid; m.p.78-80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06946473B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-7c95ec121527452d8e0cb705f94426c7 |
| Source note | uspto-grants-2005_09 |