HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chlorocyclohexanone → 2-(4-Chlorophenyl)cyclohexan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chlorocyclohexanone | HCID 13203 | — |
| Reactant | HCID 178478191 | HCID 178478191 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(4-Chlorophenyl)cyclohexan-1-one | HCID 3839566 | 73.8% |
Reaction Steps
A solution of 4-chlorophenylmagnesium bromide (200 mL of 1 M in ether, 200 mmol) was cooled in an ice-bath and a solution of 2-chlorocyclohexanone (26.5 g, 200 mmol) in 200 mL of ether was slowly added. The mixture was stirred at room temperature for 4 hours and was then concentrated under reduced pressure. Benzene (300 mL) was added and the mixture was heated under reflux for 12 h. Dilute aqueous HCl was added and the organic layer was separated, washed with brine, dried (sodium sulfate) and evaporated. Bulb-to-bulb distillation (2 mm) afforded 30.8 g of liquid product that subsequently crystallized.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07223767B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-a614873a65dd4c50b079bde0cf9bd5d0 |
| Source note | uspto-grants-2007_05 |