use | 2,3,4,5, 6-pentafluorobenzyl chloride can be used as an intermediate in pharmaceutical synthesis, can be prepared by the reaction of hexafluorobenzene and methyl lithium, and can be used to prepare 2,3,4,5, 6-pentafluorobenzyl cyanide. |
preparation | add an ether solution of methyl lithium (70cc, containing 21g of methyl lithium) to hexafluorobenzene (20g) in the dry ether (20cc) at a rate sufficient to maintain mild reflux, stir, after adding and adding water (100cc), keep stirring for one hour. The ether layer was dried (MgSO4), filtered, and most of the ether was distilled off by a 6-inch column, and the residual liquid (17g) was separated, and 2,3,4,5, 6-pentafluorotoluene (138g) was obtained by gas chromatograph 100 (column 488 cmx75mm, filled with silicone rubber/diatomite 1:3, temperature 1000°C, no flow 451/hr). The methyl halogenation is then reacted with one molecular equivalent of sulfonyl chloride in the presence of 0005 molecular equivalent of dibenzoyl peroxide. The main product is 2,3,4,5, 6-pentafluorobenzyl chloride, boiling point 88-90°C, mercury pressure 69mm. |