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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Ethyl-2-fluoro-1,1'-biphenyl | HCID 1490326 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1,1'-Biphenyl, 4-ethenyl-2-fluoro- | HCID 11424166 | 55.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04329507 |
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| Source dataset | uspto-grants-1982_05 |
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| ORD ID | ord-6d1c0c0891be49f1bf021e2c2febd442 |
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| Source note | uspto-grants-1982_05 |
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