HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Ethylaniline → 2-[Ethyl(phenyl)amino]ethane-1-sulfonyl fluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Ethylaniline | HCID 7670 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethanesulfonyl fluoride, 2-chloro- | HCID 69807 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 2-[Ethyl(phenyl)amino]ethane-1-sulfonyl fluoride | HCID 21161687 | — |
Reaction Steps
N-Ethylaniline (48.4 g 0.4 m), triethylamine (40.4 g 0.4 m) and benzene (100 ml) are stirred together at room temperature and 2-chloroethanesulfonyl fluoride (58.6 g, 0.4 m) is added dropwise. The reaction mixture is heated at reflux for 1.5 hr. after the addition is completed. The reaction mixture is cooled and filtered to remove any insoluble salts, and the benzene is removed by distillation. The crude product is drowned into hexane (150 ml) and purified by filtration and washing with hexane. The product melts at 48°-50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04282144 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-81e06920a49f4661a6f671681dad4846 |
| Source note | uspto-grants-1981_08 |