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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-[1,1'-biphenyl]-2-carboxaldehydeHCID 13216679—
ReactantButyllithiumHCID 178418339—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product3-Chloro-2-ethenyl-1,1'-biphenylHCID 1285305153.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04402973
Source datasetuspto-grants-1983_09
ORD IDord-ef5e7d69196944b4b4ae5938d9ba7474
Source noteuspto-grants-1983_09