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 | Epichlorohydrin | HCID 7835 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Solvent | Water | HCID 962 | — |
| Product | N,N-bis(2-oxiranylmethyl)benzenesulfonamide | HCID 11207928 | 46% |
Reaction Steps
This reaction is very exothermic so care must be taken if the reaction is scaled up. Acetonitrile (400 mL) and (±)-epichlorohydrin (100 mL, 118.3 g, 0.78 mol) were added to benzenesulfonamide (50.0 g, 0.32 mol), followed by cesium carbonate (228 g, 0.70 mol). The mixture was heated at reflux for 15 hours with mechanical stirring. After cooling to room temperature water was added (250 mL) and the organic phase separated and concentrated under reduced pressure. The residual oil was chromatographed over silica (300 g), eluting with dichloromethane (1 L) and then dichloromethane:ethyl acetate (3 L of 19:1), to give the sub-title compound as an oil (39.4 g, 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772229B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-40f797321bd0451db25fcdaf0e83b71c |
| Source note | uspto-grants-2010_08 |