HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266445Generated: October 31, 2026
Chloromethyl phenyl sulphide → HCID 70044820, compound
https://huagongshe.com/reaction/266445
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloromethyl phenyl sulphide | HCID 81623 | — |
| Reactant | 133743-22-3 | HCID 14257493 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 70044820 | HCID 70044820 | 84% |
Reaction Steps
A mixture of 3.27 g (0.012 mol) of 4-bromosaccharin [Japanese Pat. Publcn. 58/79,034, published May 12, 1983; C. A. 100, 7773w (1984)], 1.63 g (0.015 mol) of potassium t-butoxide, 0.39 g (0.0012 mol) of tetrabutylammonium bromide and 3.0 ml (0.022 mol) of chloromethyl phenyl sulfide in 100 ml of toluene was heated under reflux under a nitrogen atmosphere for eight hours and then at ambient temperature for about sixteen hours. The reaction mixture was then cooled, diluted with ethyl acetate and the organic layer washed with bicarbonate, water and brine and then dried over magnesium sulfate and taken to dryness in vacuo. The residual solid was recrystallized from toluene-hexane to give 3.86 g (84%) of 4-bromo-2-phenylthiomethylsaccharin, mp 174.5°-178° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650422 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-03e9ebc55f2f4b84976700a702e8865d |
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| Source note | uspto-grants-1997_07 |
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