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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284910Generated: November 1, 2026

o-(Trifluoromethyl)benzaldehyde → HCID 20250823, compound

https://huagongshe.com/reaction/1284910

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-(Trifluoromethyl)benzaldehydeHCID 123067—
ReactantMethyl 3-aminocrotonateHCID 643918—
ReactantHCID 20250815HCID 20250815—
SolventIsopropanolHCID 3776—
ProductHCID 20250823HCID 20250823—

Reaction Steps

13.2 Grams of o-trifluoromethylbenzaldehyde, 14.6 g of 4-chlorobutyl acetoacetate and 8.8 g of methyl 3-aminocrotonate were added to 50 ml of isopropanol, and the whole mixture was refluxed by heating for 4 hours. The reaction mixture was concentrated, and the residue was purified by a silica gel column chromatography (eluant=chloroform) to yield 18.2 g of 4-chlorobutyl methyl 1,4-dihydro-2,6-dimethyl-4-(2-trifluoromethylphenyl)pyridine-3,5-dicarboxylate in the form of yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04564619
Source datasetuspto-grants-1986_01
ORD IDord-b4b105fdf9694e1e856d682112ad45d9
Source noteuspto-grants-1986_01