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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308915Generated: November 1, 2026

Hydrochloric Acid → Diethyl 2-(difluoromethyl)-4-ethyl-6-(trifluoromethyl)-3,5-pyridinedicarboxylate

https://huagongshe.com/reaction/2308915

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-Dihydro-2,6-bis(trifluoromethyl)-4-ethylpyridine-3,5-dicarboxylic acid diethyl esterHCID 13957621—
Reactant1,2,3,4,6,7,8,10A-octahydropyrimido[1,2-a]azepineHCID 15072656—
SolventTetrahydrofuranHCID 8028—
ProductDiethyl 2-(difluoromethyl)-4-ethyl-6-(trifluoromethyl)-3,5-pyridinedicarboxylateHCID 1395765778.5%

Reaction Steps

A mixture of 1558 g (4.00 moles) of diethyl 2,6-bis(trifluoromethyl)-1,4-dihydro-4-ethyl-3,5-pyridinedicarboxylate, 628 g (4.0 moles) of 1,8-diazabicyclo-[5.4.0]-undec-5-ene (DBU), and 500 ml of tetrahydrofuran is held at reflux for 19 hours, cooled and poured into a mixture of 2 kg of ice and 250 ml of concentrated hydrochloric acid. The organic layer is separated and the aqueous layer extracted with 500 ml of CH2Cl2 twice. The combined organic materials are dried (MgSO4) and concentrated. The residue is kugelrohr distilled at 1 torr (pot temperature of 150°-160° C.) to give 1158 g (78.5%) of desired product, nD25 1.4458.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04692184
Source datasetuspto-grants-1987_09
ORD IDord-376afb25b59a489e8a953dc60bdb4311
Source noteuspto-grants-1987_09