Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 4-Trifluoromethoxy-biphenyl | HCID 10889960 | — |
| Solvent | Nitrobenzene | HCID 7416 | — |
| Product | HCID 86759746 | HCID 86759746 | — |
Reaction Steps
To a mixture of 30 g (126 mmol) 4-(trifluoromethoxy)-1,1′-biphenyl and 21 g aluminium trichloride (157 mmol) in 120 ml nitrobenzene are added at a temperature below 20° C. 9.87 g (126 mmol) acetyl chloride. The reaction mixture is stirred for 2 h at 0° C., added to 240 ml ice-water and 42 ml conc. HCl and extracted with ethyl acetate. The organic phase is washed with water and brine and the solvents removed in vacuo. The residue is triturated with petrol ether, filtrated and dried. From the filtrate another batch can be obtained after crystallizing at 4° C. to give overall 23.5 g (66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06900194B1 |
|---|
| Source dataset | uspto-grants-2005_05 |
|---|
| ORD ID | ord-3397441bae354d209d5f4068d948b263 |
|---|
| Source note | uspto-grants-2005_05 |
|---|