HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chlorobenzene → 4-CHLOROPHENYL CYCLOHEXYL KETONE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chlorobenzene | HCID 7964 | — |
| Reactant | Cyclohexanecarbonyl chloride | HCID 75938 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 4-CHLOROPHENYL CYCLOHEXYL KETONE | HCID 11579456 | — |
Reaction Steps
To a mixture of 80 ml (0.78 mol) of chlorobenzene and 30 g (0.22 mol) of aluminium chloride are added dropwise at 15-20° C. 24 ml (0.18 mol) of cyclohexanecarboxylic acid chloride. After one hour at ambient temperature the reaction mixture is heated for 5 hours to 50° C. After cooling, the mixture is then decomposed with ice water/conc. hydrochloric acid and the aqueous phase is extracted with methylene chloride. The combined organic extracts are dried and evaporated down. The residue is distilled under high vacuum (2 mm, 105-115° C.). The desired fraction is combined with water, the precipitate formed is suction filtered and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06114532 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-099f75450912463a90087ed52bc32345 |
| Source note | uspto-grants-2000_09 |