HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfenyl chloride → 2-(m-Chlorophenyl)-5-(phenylthio)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfenyl chloride | HCID 11008040 | — |
| Reactant | 2-(3-Chlorophenyl)thiophene | HCID 12362444 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(m-Chlorophenyl)-5-(phenylthio)thiophene | HCID 20386607 | 22% |
Reaction Steps
A mixture of 89 g (0.46 mole) of 2-(m-chlorophenyl)thiophene, 400 ml of reagent carbon tetrachloride, 54 ml (67 g, 0.46 mole) of benzenesulfenyl chloride and 0.05 g of iron powder was allowed to stand for four days at room temperature. A further 12 ml (15 g, 0.10 mole) of benzenesulfenyl chloride and 0.05 g of iron powder were added. After four days the carbon tetrachloride was removed by distillation. The residue was distilled at reduced pressure to give 30 g (22%) of 2-(m-chlorophenyl)-5-(phenylthio)thiophene, b.p. 200°-205° C. (0.15 mm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174405 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-e3cd56a17f6946528e527b3512c871fa |
| Source note | uspto-grants-1979_11 |