HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → (2,4-Dimethyl-phenyl)-(4-fluoro-phenyl)-methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | M-Xylene | HCID 7929 | — |
| Reactant | 4-Fluorobenzoyl chloride | HCID 67879 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | (2,4-Dimethyl-phenyl)-(4-fluoro-phenyl)-methanone | HCID 10242880 | 99% |
Reaction Conditions
| Temperature | 5 °C |
|---|
Reaction Steps
To a suspension of anhydrous aluminum chloride (19.5 g) dispersed in m-xylene (150 ml) was added dropwise 4-fluorobenzoyl chloride (21.1 g) under ice-cooling. The mixture was stirred at 0-10° C. for 3 hr and poured into 6N hydrochloric acid. The reaction mixture was partitioned and the obtained organic layer was washed successively with water, 10% aqueous sodium hydroxide solution and water. The solvent was evaporated to give a 96:4 mixture (30.2 g, 99%) of 1,3-dimethyl-4-(4′-fluorobenzoyl)benzene and 1,3-dimethyl-2-(4′-fluorobenzoyl)benzene as pale-yellow oil. 1,3-Dimethyl-4-(4′-fluorobenzoyl)benzene
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06946564B2 |
| Source dataset | uspto-grants-2005_09 |
| ORD ID | ord-1d1558e1131744fa956f61b75ee3afdd |
| Source note | uspto-grants-2005_09 |