HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloride → 1,2,3,4-Tetrafluoro-5-(trichloromethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1,2,3,4-Tetrafluoro-5-(trifluoromethyl)benzene | HCID 2733690 | — |
| Product | 1,2,3,4-Tetrafluoro-5-(trichloromethyl)benzene | HCID 15346007 | — |
Reaction Steps
85 g (0.64 mol) of aluminiumn chloride (anhydrous) are initially introduced into 500 ml of methylene chloride, and 109 g (0.5 mol) of 2,3,4,5-tetrafluoro-benzotrifluoride are added dropwise at room temperature, while stirring. The, mixture is then subsequently stirred at 40° C. for 1 hour, allowed to cool and poured onto 600 g of ice, the organic phase is separated off, the aqueous phase is extracted with ether and the combined phases are washed with water and dried over anhydrous magnesium sulphate. After concentration, the residue is distilled. 108.3 g (81% of theory) of product are obtained; boiling point: 89-90° C./22 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06075165 |
| Source dataset | uspto-grants-2000_06 |
| ORD ID | ord-2ec7e7a559cd47c9ad31adbae252b74e |
| Source note | uspto-grants-2000_06 |