HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-[(3,4-dichlorophenyl)amino]ethanesulfonyl Fluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3,4-Dichloroaniline | HCID 7257 | — |
| Reactant | Ethenesulfonyl fluoride | HCID 69612 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-[(3,4-dichlorophenyl)amino]ethanesulfonyl Fluoride | HCID 4738192 | — |
Reaction Steps
A N,N-dimethylformamide solution (DMF, 100 ml) of 3,4-dichloroaniline (6.48 g, 40 mmol) and ethenesulfonyl fluoride (6.7 g, 57.9 mmol) was warmed to 110° C. for three hours. The cooled dark solution was diluted to 400 ml with water and the resulting dark oily precipate was decanted from the supernatant layer. This layer was extracted with ether (4×50 ml). The combined ether extracts were added to the oily precipitate and this dark solution was washed with brine and dried over MgSO4. The organic solution was evaporated to give the crude 2-[(3,4-dichlorophenyl)amino]ethanesulfonyl fluoride as a dark liquid in quantitative yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04874771 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-bd90fc6bb6bd479d855c74b35a1f492e |
| Source note | uspto-grants-1989_10 |