HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfenyl chloride → 2-p-Anisyl-5-(phenylthio)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfenyl chloride | HCID 11008040 | — |
| Reactant | 2-(4-Methoxybenzyl)thiophene | HCID 11030941 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-p-Anisyl-5-(phenylthio)thiophene | HCID 20386645 | 29% |
Reaction Steps
A solution of 34 g (0.179 mole) of 2-p-anisylthiophene in 500 ml of carbon tetrachloride was treated with 23 ml (28.5 g, 0.197 mole) of benzenesulfenyl chloride and 0.1 g of iron powder. The mixture was allowed to stand at room temperature for eight days. The mixture was filtered to remove a small amount of solid. The filtrate was evaporated to give 67 g of crude solid product. Recrystallization from 220 ml of ethyl acetate gave 15.4 g (29%) of 2-p-anisyl-5-(phenylthio)thiophene, m.p. 92°-93° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174405 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-b702cd1924054e6f97e089e9f9f5781a |
| Source note | uspto-grants-1979_11 |