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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290315Generated: November 1, 2026

2,3-Dichlorobenzaldehyde → HCID 13457175, compound

https://huagongshe.com/reaction/2290315

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-DichlorobenzaldehydeHCID 35745—
ReactantMethyl 3-aminocrotonateHCID 643918—
ReactantHCID 13457163HCID 13457163—
SolventMethanolHCID 887—
ProductHCID 13457175HCID 1345717546.7%

Reaction Steps

A solution of 2,3-dichlorobenzaldehyde (8.75 g), methyl 3-aminocrotonate (5.75 g) and ethyl 4-[2-(2,4,5-trimethyl-1-imidazolyl)ethoxy]acetoacetate (14.1 g) in 50 ml of methanol was stirred at reflux temperature for 5 hours. After evaporation to dryness, the residue was dissolved in 2N hydrochloric acid (200 ml) and washed with diethyl ether (3×100 ml) followed by extraction with methylene chloride (4×150 ml). The combined methylene chloride extracts were washed with saturated aqueous sodium carbonate solution (2×200 ml), dried (Na2CO3), filtered and evaporated to give a beige solid (12.5 g). The crude product was chromatographed on silica (40 g), eluting with ethyl acetate. The appropriate fractions were combined and evaporated and the resultant oil (2.1 g) crystallised from diethyl ether (10 ml) to give the title compound, (1.5 g), m.p. 123°-125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04616024
Source datasetuspto-grants-1986_10
ORD IDord-5d689a857c2a477885e924c00ac8fc3b
Source noteuspto-grants-1986_10