HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Chlorothiophenol → 3,4,5-Tris-(p-chlorophenylthio)-6-bromophthalimide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Chlorothiophenol | HCID 7815 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,4,5,6-Tetrabromophthalimide | HCID 90490 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4,5-Tris-(p-chlorophenylthio)-6-bromophthalimide | HCID 20269586 | 25.1% |
Reaction Steps
2 g (4.46 millimols) of tetrabromophthalimide, 1.61 g (11.15 millimols) of p-chlorothiophenol, 2.31 g (16.73 millimols) of potassium carbonate and 20 ml of tetrahydrofuran are stirred at 25° C. for 14 hours. After acidification with dilute HCl solution, the mixture is extracted with tetrahydrofuran/toluene and the extracts are dried and evaporated. After recrystallisation from toluene/cyclohexane, 0.61 g (25% of theory) of 3,4,5-tris-(p-chlorophenylthio)-6-bromophthalimide is obtained; melting point 164°-9° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04537977 |
| Source dataset | uspto-grants-1985_08 |
| ORD ID | ord-37a60ba89cdb4c098ddd35a1a33dd0e4 |
| Source note | uspto-grants-1985_08 |