Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609574Generated: October 29, 2026

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

https://huagongshe.com/reaction/1609574

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 absolution 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 numberUS05401746
Source datasetuspto-grants-1995_03
ORD IDord-5a32d8f2ad324dd28871153b57aacb02
Source noteuspto-grants-1995_03