Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295183Generated: October 30, 2026

HCID 19867638, compound → HCID 14460148, compound

https://huagongshe.com/reaction/2295183

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19867638HCID 19867638—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
ProductHCID 14460148HCID 1446014877.8%

Reaction Steps

A slurry of LiAlH4 (775 mg, 20.4 mmol) in dry Et2O (70 ml) at 0° C. was treated with a solution of 4-(4-fluorophenyl)-2-(1-methylethyl)-6-phenyl-3-pyridinecarboxylic acid, ethyl ester (4.80 gm, 13.2 mmol) in Et2O (5 ml). After 2.5 hours, the reaction was quenched and diluted with H2O and the aqueous layer was extracted twice with Et2O and once with EtOAc. The combined organic layers were washed with H2O and brine, then dried (Na2 SO4), filtered and stripped. The resulting solid was dissolved in hot EtOAc and directly chromatographed (flash, Merck SiO2, 20% EtOAc in hexane) to give crude 4-(4-fluorophenyl)-2-(1-methylethyl)-6-phenyl-3-pyridinemethanol. Recrystallization from hot hexane/EtOAc gave 4-(4-fluorophenyl)-2-(1-methylethyl)-6-phenyl-3-pyridinemethanol (3.30 gm) as a white solid. The mother liquor was stripped and recrystallized again to give an additional 230 mg of product (total 3.53 gm, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05691322
Source datasetuspto-grants-1997_11
ORD IDord-023983f0e7c04563871c3ae8a01355fd
Source noteuspto-grants-1997_11