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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649657Generated: October 30, 2026

Hydrochloric Acid → Diethyl 2,6-bis(trifluoromethyl)-4-methoxy-3,5-pyridinedicarboxylate

https://huagongshe.com/reaction/1649657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylamineHCID 7912—
ReactantEthyl chloroformateHCID 10928—
ReactantLithium diisopropylamideHCID 2724682—
Reactant4-Methoxy-2,6-bis-trifluoromethyl-nicotinic acid ethyl esterHCID 13882866—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductDiethyl 2,6-bis(trifluoromethyl)-4-methoxy-3,5-pyridinedicarboxylateHCID 1401377675.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cold (-78° C.) solution of LDA, from 0.02 mol (2.8 ml) of diisopropylamine, 0.0208 mol of n-BuLi, and 30 ml of DME was added a solution of 4.65 g (0.015 mol) of product of Example 4 in 20 ml of DME. The resulting greenish solution was stirred at -78° C. for 10 minutes and treated with 2.7 ml (0.035 mol) of ethyl chloroformate. The reaction mixture was warmed to room temperature in 40 minutes, then poured into a mixture of 20 ml of concentrated HCl and 50 ml of water. The mixture was extracted with ether (200 ml). The ether extract was dried and concentrated. The residue was kugelrohr distilled at 13 Pa. The earlier fraction (pot temperature 50°-65° C.) was discarded. The later fraction (pot temperature 90° C.) was an oil (5.47 g) which was crystallized from hexane at low temperature to give 4.4 g (75%) of product; mp 46.5°-47.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04921530
Source datasetuspto-grants-1990_05
ORD IDord-951e4010df13437c9835041e3e7662b9
Source noteuspto-grants-1990_05