HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Bromophenyl)thiophene → 2-(p-Bromophenyl)-5-(m-nitrophenylthio)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Bromophenyl)thiophene | HCID 7018298 | — |
| Reactant | 1-(Chlorosulfanyl)-3-nitrobenzene | HCID 15620686 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(p-Bromophenyl)-5-(m-nitrophenylthio)thiophene | HCID 20386659 | 44% |
Reaction Steps
To a solution of 21.2 g (0.112 mole) of m-nitrobenzenesulfenyl chloride in 160 ml of carbon tetrachioride were added 24.5 g (0.103 mole) of 2-(p-bromophenyl)thiophene and 0.1 g of iron powder. The reaction mixture was allowed to stand one week at room temperature. Evaporation of the solvent and recrystallization of the residue from 140 ml of ethyl acetate gave 17.6 g (44%) of 2-(p-bromophenyl)-5-(m-nitrophenylthio)thiophene, m.p. 120°-122° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04174405 |
| Source dataset | uspto-grants-1979_11 |
| ORD ID | ord-362563c75c84490c9f528892d920a28b |
| Source note | uspto-grants-1979_11 |