HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → 4-Chloro-4'-ethylthiomethylbenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Chloro-4'-mercaptomethylbenzophenone | HCID 19689380 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Chloro-4'-ethylthiomethylbenzophenone | HCID 19689354 | 79.1% |
Reaction Steps
4-chloro-4'-mercaptomethylbenzophenone (16.0 g), ethyl bromide (7.4 g) and potassium hydroxide (4.3 g) were added to methanol (250 ml), and the mixture was stirred for 30 minutes under reflux. The reaction mixture was cooled to room temperature and then concentrated. Water was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with water and then dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=10:1) to obtain the desired product 14.0 g, melting point: 33° to 34° C., yield: 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05728699 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-854622046616431a8dec648c46bb4905 |
| Source note | uspto-grants-1998_03 |