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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890151Generated: October 30, 2026

3-Chlorobenzaldehyde → HCID 69071615, compound

https://huagongshe.com/reaction/890151

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorobenzaldehydeHCID 11477—
ReactantBenzyl acetoacetateHCID 142266—
Reactant2-Cyanoethyl 3-aminocrotonateHCID 13671410—
SolventIsopropanolHCID 3776—
ProductHCID 69071615HCID 69071615—

Reaction Steps

3.53 g (22.9 mmol) of 2-cyanoethyl 3-aminocrotonate, 4.40 g (22.9 mmol) of benzyl acetoacetate and 2.60 ml (23.0 mmol) of 3-chlorobenzaldehyde were heated at 80° C. under stirring in 100 ml of 2-propanol for 3 days. 2-Propanol was evaporated under reduced pressure to obtain 5-benzyl 3-(cyanoethyl) 4-(3-chlorophenyl)-2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate. 100 ml of ethyl acetate and 10% palladium/carbon were added to the reaction mixture, and they were stirred at room temperature in hydrogen atmosphere under atmospheric pressure for 7 days. The reaction liquid was filtered. The filtrate was evaporated under reduced pressure. The residue was washed with chloroform to obtain the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995179B2
Source datasetuspto-grants-2006_02
ORD IDord-ad909f1c955141ce946e829f1b06b6f1
Source noteuspto-grants-2006_02