Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236571Generated: October 26, 2026

2-Chlorobenzaldehyde → HCID 13564978, compound

https://huagongshe.com/reaction/236571

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzaldehydeHCID 6996—
Reactant2-Propanone, 1-nitro-HCID 66296—
ReactantHCID 21278157HCID 21278157—
SolventEthanolHCID 702—
ProductHCID 13564978HCID 13564978—

Reaction Steps

28.1 g (200 mmol) of 2-chlorobenzaldehyde are boiled under reflux with 37.4 g (200 mmol) of 2-acetoxyethyl β-aminocrotonate and 32.6 g (320 mmol) of nitroacetone in 400 ml of ethanol for 4 hours. The mixture is cooled and concentrated. The evaporation residue is taken up in ethyl acetate and the mixture is washed with water, sodium bicarbonate solution and water again, dried and concentrated. The semi-solid evaporation residue is stirred with ethanol, filtered off with suction and washed with ethanol. 23.2 g (29.4% of theory) of a yellow-colored product of melting point 158°-160° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04645775
Source datasetuspto-grants-1987_02
ORD IDord-09dfd876ef0a4019949835f7b55cc85e
Source noteuspto-grants-1987_02