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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681267Generated: November 2, 2026

Ethanol → Ethyl 2,6-diisopropyl-5-ethoxymethyl-4-(4-fluorophenyl)pyridine-3-carboxylate

https://huagongshe.com/reaction/1681267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium hydrideHCID 24758—
ReactantEthyl 5-chloromethyl-2,6-diisopropyl-4-(4-fluorophenyl)pyridine-3-carboxylateHCID 20081869—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2,6-diisopropyl-5-ethoxymethyl-4-(4-fluorophenyl)pyridine-3-carboxylateHCID 20081845—

Reaction Steps

4.4 ml (76 mmol) of absolute ethanol are added dropwise at room temperature to a suspension of 2.29 g (76 mmol) of sodium hydride (80% strength) in 30 ml of absolute tetrahydrofuran and the mixture is stirred for 30 minutes. A solution of 2.7 g (7.6 mmol) of the compound from Example 86 are then added dropwise in 20 ml of absolute tetrahydrofuran and the mixture is heated overnight under reflux. The reaction batch is subsequently poured onto ice water and, after the pH has been adjusted to 8, extracted several times using ether. The organic phase is washed with sodium chloride solution, dried over sodium sulphate, concentrated and chromatographed over silica gel (eluent ethyl acetate/petroleum ether 5195).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05169857
Source datasetuspto-grants-1992_12
ORD IDord-17d527ace4504181a6638b7c3efdb527
Source noteuspto-grants-1992_12