HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → N-benzyloxy-3-chloropropylsulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloropropanesulphonyl chloride | HCID 15410 | — |
| Reactant | Benzyloxyamine hydrochloride | HCID 102312 | — |
| Catalyst | Bis(tetrabutylammonium) sulphate | HCID 11433187 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-benzyloxy-3-chloropropylsulfonamide | HCID 10539517 | 41% |
Reaction Steps
3-Chloropropylsulfonyl chloride 1 (30.28 g,0.17 mol), O-benzylhydroxylamine hydrochloride (27.3 g,0.17 mol), potassium carbonate (50 g,0.36 mol) and tetrabutylammonium sulfate (about 500 mg) are reacted with each other in a mixture of ether and water (1:1) (100 ml) for 24 hours at room temperature and the reaction mixture was extracted with ethyl acetate. The extract was subjected to column chromatography on silica gel. From the fraction eluted with a mixture of ethyl acetate/n-hexane (1:4),18.4 g (41%) of crude N-benzyloxy-3-chloropropylsulfonamide (intermediate 3g) was obtained as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05418230 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-ffa5db23b6c645ea926f7c0af8d36b34 |
| Source note | uspto-grants-1995_05 |