HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → N,N-bis(2-oxiranylmethyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (-)-Epichlorohydrin | HCID 2734062 | — |
| Solvent | Water | HCID 962 | — |
| Product | N,N-bis(2-oxiranylmethyl)benzenesulfonamide | HCID 11207928 | 43% |
Reaction Steps
This reaction is very exothermic so care must be taken if the reaction is scaled up. Acetonitrile (100 mL) and (R)-(−)-epichlorohydrin (47 mL, 55.6 g, 0.60 mol) were added to benzenesulfonamide (20.0 g, 0.127 mol), followed by cesium carbonate (83 g, 0.255 mol). The mixture was heated at reflux for 6 hours with mechanical stirring and then was stirred overnight at room temperature. Water was added (100 mL), the organic phase separated and then concentrated under reduced pressure. The residual oil was chromatographed over silica, eluting with dichloromethane then dichloromethane:ethyl acetate (19:1), to give the sub-title compound as an oil (14.8 g, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772229B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-f98d6ff45d124371959d012aa2c20386 |
| Source note | uspto-grants-2010_08 |