HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfenyl chloride → 2-Phenylthio-5-(3,4-xylyl)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfenyl chloride | HCID 11008040 | — |
| Reactant | 2-(3,4-Xylyl)thiophene | HCID 19905009 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Phenylthio-5-(3,4-xylyl)thiophene | HCID 20386655 | 29.1% |
Reaction Steps
A mixture of 37 g (0.197 mole) of 2-(3,4-xylyl)thiophene, 200 ml of reagent carbon tetrachloride, 29 ml (36 g, 0.259 mole) of benzenesulfenyl chloride and 0.05 g of iron powder was allowed to stand two days at room temperature. A vapor phase chromatogram of the mixture showed that all the 2-(3,4-xylyl)thiophene had been consumed. The carbon tetrachloride was removed by distillation and the residue recrystallized from ethanol to give a first crop of 17 g (29%) of 2-phenylthio-5-(3,4-xylyl)thiophene, m.p. 77°-78° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174405 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-f4ee1ab59c0149929c9669971a4cb76b |
| Source note | uspto-grants-1979_11 |