HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → (4-Cyclohexylphenyl)(phenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Cyclohexylbenzene | HCID 13229 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Cyclohexylphenyl)(phenyl)methanone | HCID 265880 | 75% |
Reaction Steps
67 g (0.5 mol) of aluminium chloride are added in portions to a mixture of 80 g (0.5 mol) of cyclohexylbenzene 70 g (0.5 mol) of benzoyl chloride and 500 ml of methylene chloride at room temperature. After 15 hours, the reaction mixture is poured onto ice/hydrochloric acid. The organic phase is washed with water until neutral, dried over sodium sulphate and evaporated. The crude product is purified by distillation. 93.3 g (75% of theory) of 4-cyclohexylbenzophenone of boiling point 160° to 175° C./0.1 mm are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04238498 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-8f91a212420449fbb3fffc75dd7d4e02 |
| Source note | uspto-grants-1980_12 |