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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905247Generated: October 30, 2026

Pentafluorobenzyl bromide → Pentafluoro-benzyl 2,2-dimethyl-3-(2-chloro-2-p-chloro-phenyl-vinyl)-cyclopropanecarboxylate

https://huagongshe.com/reaction/905247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentafluorobenzyl bromideHCID 74484—
ReactantPotassiumHCID 5462222—
ReactantHCID 54156496HCID 54156496—
SolventDimethylformamideHCID 6228—
ProductPentafluoro-benzyl 2,2-dimethyl-3-(2-chloro-2-p-chloro-phenyl-vinyl)-cyclopropanecarboxylateHCID 13171332574.4%

Reaction Steps

10.7 g (0.033 mol) of the potassium salt of 2,2-dimethyl-3-(2-chloro-2-p-chlorophenyl-vinyl)-cyclopropanecarboxylic acid were dissolved in 100 ml of dimethylformamide and the solution was heated to 120° C., together with 6.8 g (0.026 mol) of pentafluorobenzyl bromide, for 3 hours. After the reaction had ended, the dimethylformamide was distilled off in vacuo and the residue which remained was taken up in 200 ml of methylene chloride. The methylene chloride solution was then extracted by shaking twice with 100 ml of water each time, the organic phase was dried over sodium sulphate and the solvent was stripped off in vacuo. Last residues of solvent were removed by brief incipient distillation at a bath temperature of 60° C./1 mm Hg. 9.0 g (74.4% of theory) of pentafluoro-benzyl 2,2-dimethyl-3-(2-chloro-2-p-chloro-phenyl-vinyl)-cyclopropanecarboxylate were obtained as a yellow oil with the refractive index nD25 :1.5382.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04423066
Source datasetuspto-grants-1983_12
ORD IDord-93692779fc2842c4921ffe45406ef841
Source noteuspto-grants-1983_12