HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995130Generated: October 30, 2026
3-Chloro-[1,1'-biphenyl]-2-carboxaldehyde → 3-Chloro-2-ethenyl-1,1'-biphenyl
https://huagongshe.com/reaction/1995130
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-[1,1'-biphenyl]-2-carboxaldehyde | HCID 13216679 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Chloro-2-ethenyl-1,1'-biphenyl | HCID 12853051 | 53.6% |
Reaction Steps
Under a dry argon atmosphere n-butyllithium (1.3 g, 0.020 mole) was added slowly to a stirred ice cold mixture of (methyl)triphenylphosphonium bromide (7.3 g, 0.0203 mole) in 30 ml of tetrahydrofuran. The mixture was warmed to room temperature, stirred for two hours, and 3-chloro-[1,1'-biphenyl]-2-carboxaldehyde (4.4 g, 0.0203 mole) in 30 ml of tetrahydrofuran added. The reaction mixture was stirred at room temperature for approximately 18 hours, heated at reflux for two hours, then cooled. The reaction mixture was diluted with 300 ml of diethyl ether and washed with 100 ml of water. The organic phase was dried over anhydrous magnesium sulfate, filtered, and evaporated to give a residue. Distillation of the residue at 88°/0.05 mm gave 3-chloro-2-ethenyl-[1,1'-biphenyl] (2.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04402973 |
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| Source dataset | uspto-grants-1983_09 |
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| ORD ID | ord-ef5e7d69196944b4b4ae5938d9ba7474 |
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| Source note | uspto-grants-1983_09 |
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