HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Phenylsulphenyl-4-trifluoromethylbenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Nitro-4-(trifluoromethyl)benzonitrile | HCID 69902 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Phenylsulphenyl-4-trifluoromethylbenzonitrile | HCID 18977984 | 85.2% |
Reaction Steps
A mixture of 2-nitro-4-trifluoromethylbenzonitrile (8.64 g), thiophenol (4.4 g) and potassium carbonate (6.9 g) in acetonitrile was heated at reflux for 4 hours. After cooling, the mixture was poured into water and extracted with dichloromethane. The organic extract was dried over anhydrous sodium sulphate, filtered and concentrated under reduced pressure. The residue was triturated with hexane to give 2-phenylsulphenyl-4-trifluoromethylbenzonitrile as a white solid (9.5 g), m.p. 51° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05371064 |
| Source dataset | uspto-grants-1994_12 |
| ORD ID | ord-17b8395c8a9c4cb2ab4afbfeff5407c5 |
| Source note | uspto-grants-1994_12 |