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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324790Generated: October 30, 2026

Water → Ethyl 2,6-Diisopropyl-4-(4-fluorophenyl)-3-hydroxymethylpyridine-5-carboxylate

https://huagongshe.com/reaction/324790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiethyl 2,6-diisopropyl-4-(4-fluorophenyl)-pyridine-3,5-dicarboxylateHCID 10179180—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2,6-Diisopropyl-4-(4-fluorophenyl)-3-hydroxymethylpyridine-5-carboxylateHCID 10291957—

Reaction Conditions

Temperature0 °C

Reaction Steps

257 ml (0.9 mol) of a 3.5 molar solution of sodium-bis-(2-methoxy-ethoxy)dihydroaluminate is steadily added by drops under nitrogen to a solution of 120 g (0.3 mol) of the compound from Example VIII in 800 ml of dried tetrahydrofuran at room temperature, and the mixture is subsequently stirred for 5 h. After cooling to 0° C., 500 ml of water is carefully added by drops, the phases are separated, and the aqueous phase is extracted three times with 250 ml ethyl acetate each time. The combined organic phases are washed with saturated sodium chloride solution, dried over magnesium sulfate, and evaporated in a vacuum. The residue is mixed with petroleum ether, drawn off by suction, and dried in a desiccator.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218431B1
Source datasetuspto-grants-2001_04
ORD IDord-2d2fe669d3b44e6b9af94d66818dcb18
Source noteuspto-grants-2001_04