HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 2-Phenylthiomethyl-4-sec-butyl-6-methoxysaccharin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Phenylchloromethyl sulfide | HCID 20138743 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 4-Sec-butyl-6-methoxysaccharin | HCID 67784561 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Product | 2-Phenylthiomethyl-4-sec-butyl-6-methoxysaccharin | HCID 67784306 | 60% |
Reaction Steps
A mixture of 4-sec-butyl-6-methoxysaccharin (3 g), toluene, potassium t-butoxide (1.4 g), and tetrabutylammonium bromide (0.4 g) was brought to reflux and phenylchloromethyl sulfide (1.8 mL) was added. The reaction mixture was refluxed for about 27 hours, the solvent was removed in vacuo, the residue was extracted with ethyl acetate, washed with brine and dried over Na2SO4. The solvent was removed in vacuo and the residue was purified by column chromatography on silica eluting with 10% ethyl acetate/hexane to afford 2.63 g (60%) of 2-phenylthiomethyl-4-sec-butyl-6-methoxysaccharin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05466701 |
| Source dataset | uspto-grants-1995_11 |
| ORD ID | ord-84f738588e9e4ac995771c12a62e54f0 |
| Source note | uspto-grants-1995_11 |