HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 4-Methoxybenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | 4-Methoxybenzophenone | HCID 69146 | 90.1% |
Reaction Steps
To an agitated mixture of lithium Chloride (3.18 g., 0.075 mole) and aluminium chloride (20 g., 0.15 mole) in dichloroethane cooled to below -10° C. was added anisole (5.41 g.,-0.05 mole) and benzoyl chloride (7.03 g., 0.05 mole) in dichloroethane (10ml). The reaction mixture was held below -10° C. for one hour then allowed to come to room temperature overnight. The 4-methoxybenzophenone produced (9.55 g., 90.1% yield) had a gas chromatograph/mass spectrometer estimated purity of over 95% with 2% ortho isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05068447 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-00fc8c8291844d7dbf88b4f4d1ade7b1 |
| Source note | uspto-grants-1991_11 |