Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789013Generated: October 27, 2026

2-Fluoro-6-(trifluoromethyl)benzaldehyde → 3-Methyl 5-(1-methylethyl) 2-(fluoromethyl)-4-(2-fluoro-6-(trifluoromethyl)phenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylate

https://huagongshe.com/reaction/1789013

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-6-(trifluoromethyl)benzaldehydeHCID 521933—
ReactantIsopropyl3-aminocrotonateHCID 3271821—
ReactantMethyl 4-fluoro-3-oxobutanoateHCID 14170515—
Product3-Methyl 5-(1-methylethyl) 2-(fluoromethyl)-4-(2-fluoro-6-(trifluoromethyl)phenyl)-1,4-dihydro-6-methyl-3,5-pyridinedicarboxylateHCID 141705343%

Reaction Steps

2-Fluoro-6-(trifluoromethyl)benzaldehyde (1.51 g, 7.8 mmoles), methyl 4-fluoro-3-oxobutanoate (1.06 g, 7.8 mmoles) and 1-methylethyl 3-amino-2-butenoate (1.13 g, 7.8 mmoles) were heated at 90° under nitrogen with stirring for 2 hours. The cooled reaction mixture was chromatographed twice; first eluting with toluene/ethyl acetate mixtures and then with ethyl acetate/petroleum ether (60°-80°) mixtures. The title compound (0.1 g) was obtained on evaporation of the pure fractions mp 82°-4°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04686217
Source datasetuspto-grants-1987_08
ORD IDord-bb19e9b64f2446549da75cfab4f3bd94
Source noteuspto-grants-1987_08