Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485549Generated: October 30, 2026

3-Chloro-[1,1'-biphenyl]-2-carboxaldehyde → 3-Chloro-2-ethenyl-1,1'-biphenyl

https://huagongshe.com/reaction/485549

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 numberUS04536591
Source datasetuspto-grants-1985_08
ORD IDord-5b2d50fabec54745bd16b85711b8d57c
Source noteuspto-grants-1985_08