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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1995129Generated: October 29, 2026

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

https://huagongshe.com/reaction/1995129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHexamethylenetetramineHCID 4101—
ReactantSodium ChlorideHCID 5234—
Reactant2-(Bromomethyl)-3-chloro-1,1'-biphenylHCID 13320700—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product3-Chloro-[1,1'-biphenyl]-2-carboxaldehydeHCID 13216679—

Reaction Steps

A stirred solution of 2-bromomethyl-3-chloro-[1,1'-biphenyl] (18.7 g, 0.067 mole) and hexamethylenetetraamine (9.3 g, 0.067 mole) in 200 ml of chloroform was heated at reflux for 221/2 hours. The reaction mixture was cooled and the solvent evaporated under reduced pressure to give a residue. To the residue was added 250 ml of a 1:1 solution of concentrated acetic acid:water. The mixture was heated at reflux for approximately 22 hours, then cooled. The mixture was saturated with sodium chloride and extracted with four 200 ml portions of methylene chloride. The extracts were combined, washed with saturated aqueous sodium chloride solution, followed by saturated aqueous sodium bicarbonate solution, and dried over anhydrous potassium carbonate. The mixture was filtered and the filtrate evaporated under reduced pressure to give a residue. The residue was subjected to column chromatography on silica gel, elution first with toluene:n-heptane (9:1), followed by toluene:methylene chloride (1:1), and finally methylene chloride to give 3-chloro-[1,1'-biphenyl]-2-carboxaldehyde (3.4 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04402973
Source datasetuspto-grants-1983_09
ORD IDord-64f7d5960b024a899572048292f64ede
Source noteuspto-grants-1983_09