HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylamine → N,N-diethyl-6-chlorohexanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | 6-Chlorohexanesulfonyl chloride | HCID 11063927 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N,N-diethyl-6-chlorohexanesulfonamide | HCID 22111559 | 92.8% |
Reaction Steps
6-Chlorohexanesulfonyl chloride (6.57g, 30 mmol) was added dropwise to a solution of diethyl ether (60 ml) and diethylamine (4.83g, 66 mmol) with stirring under ice-cooling. Thereafter, the mixture was stirred at the same temperature for 20 minutes. The reaction mixture was washed twice with water (10 ml) and then with brine (10 ml), and thereafter dried over anhydrous magnesium sulfate. Subsequently, the solvent was removed by evaporation In vacuo. The crude product was purified by column chromatography on silica gel with ethyl acetate-n-hexane (1:4), to give N,N-diethyl-6-chlorohexanesulfonamide (7.12 g) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172228B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-cab9efaabb284ef48d63ed856945cdea |
| Source note | uspto-grants-2001_01 |