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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065533Generated: October 27, 2026

Carbon Tetrachloride → 1,1'-Biphenyl, 4-ethenyl-2-fluoro-

https://huagongshe.com/reaction/1065533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantPotassium HydroxideHCID 14797—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Ethyl-2-fluoro-1,1'-biphenylHCID 1490326—
CatalystBenzoyl PeroxideHCID 7187—
SolventEthanolHCID 702—
Product1,1'-Biphenyl, 4-ethenyl-2-fluoro-HCID 1142416655.6%

Reaction Steps

In 750 ml. of carbon tetrachloride was dissolved 10 g of 2-fluoro-4-ethylbiphenyl. Then to the solution were added 10 g of N-bromosuccinimide and 0.1 g of benzoyl peroxide. After cooling, a solid substance was filtered off, and from the filtrate containing α-(2-fluoro-4-biphenylyl)ethyl bromide was distilled off the carbon tetrachloride. The residue thus obtained was dissolved in 500 ml. of ethyl alcohol, and then added with 17 g of potassium hydroxide. The resultant mixture was refluxed under heating for 1 hour. After cooling, the reaction mixture was poured into 2.5 l. of water, and then subjected to extraction with benzene. The benzene layer was washed with water, and dried with magnesium sulfate. The benzene in the layer was distilled off, and the resulting residue was subjected to column chromatography. From hexane eluate was obtained 5.5 g of 2-fluoro-4-vinylbiphenyl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04329507
Source datasetuspto-grants-1982_05
ORD IDord-6d1c0c0891be49f1bf021e2c2febd442
Source noteuspto-grants-1982_05