HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-Chloro-4'-ethylthiomethylbenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | S-(4-(4-chlorobenzoyl)benzyl)thiouronium bromide | HCID 18779877 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Chloro-4'-ethylthiomethylbenzophenone | HCID 19689354 | 52.2% |
Reaction Steps
S-(4-(4-chlorobenzoyl)benzyl)thiouronium bromide (3.3 g) and potassium carbonate (1.5 g) were dissolved in dimethylformnamide (20 ml). A methanol solution (10 ml) of potassium hydroxide (1.0 g) was added and stirred at room temperature for 30 minutes. To the reaction mixture, water (100 ml) and toluene (100 ml) were added. The organic layer was separated, and washed with water and an aqueous saturated sodium chloride solution, followed by drying over anhydrous magnesium sulfate. After distilling off the solvent, the crude product was purified by silica gel column chromatography (developing solvent: ethyl acetaten:hexane=1:9) to obtain 4-chloro-4'-ethylmercaptomethylbenzophenone (1.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06077866 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-54e40a5d942344f9a6b07f05d96c6218 |
| Source note | uspto-grants-2000_06 |