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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613642Generated: October 26, 2026

2-Chlorobenzaldehyde → 1-(Pyrid-3-yl)-2-(2-chlorophenyl)-2-hydroxyethanone

https://huagongshe.com/reaction/1613642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
ReactantTriethylamineHCID 8471—
Reactant3-PyridinecarboxaldehydeHCID 10371—
Catalyst3-Ethyl-5-(2-hydroxyethyl)-4-methylthiazolium bromideHCID 9964923—
SolventEthanolHCID 702—
Product1-(Pyrid-3-yl)-2-(2-chlorophenyl)-2-hydroxyethanoneHCID 19774206—

Reaction Steps

160 g (1.14 mol) of 2-chlorobenzaldehyde, 122 g (1.14 mol) of 3-pyridinealdehyde, 50 g (0.2 mol) of 3-ethyl-5-(2-hydroxyethyl)-4-methylthiazoliumbromide and 60.6 g (0.6 mol) of triethylamine in one liter of ethanol were heated at 75° C. for 13 hours. Thereafter, the ethanol was distilled off and the residue was dissolved in methylene chloride. The solution was washed twice with water and then extracted twice with 300 ml of 4N hydrochloric acid. The acidic aqueous phase was then rendered slightly alkaline with 4N sodium hydroxide solution and extracted three times with fresh methylene chloride. After the solvent had been distilled off, the crude product was stirred with isopropanol, filtered off under suction and dried to give a product of melting point 92° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194441
Source datasetuspto-grants-1993_03
ORD IDord-908219f3f9f24b2c9752eef9575872a0
Source noteuspto-grants-1993_03