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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720698Generated: November 1, 2026

tert-Butanol → HCID 21471359, compound

https://huagongshe.com/reaction/1720698

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
ReactantSodium HydroxideHCID 14798—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantHCID 14460147HCID 14460147—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 21471359HCID 21471359—

Reaction Steps

A solution of Dess-Martin periodinane (1.04 gm, 2.45 mmol) in dry CH2Cl2 (12 ml) was treated with t-butanol (182 mg, 2.46 mmol) and stirred at room temperature for 15 minutes. A slurry of 4-(4-fluorophenyl)-2-methyl-6-phenyl-3-pyridinemethanol (555 mg, 1.89 mmol) in CH2Cl2 (10 ml) and CH3CN (2 ml) was then added and stirring was continued for 25 minutes. The mixture was diluted with Et2O (50 ml) and poured into 1N NaOH (25 ml) and stirred for 5 minutes. The phases were separated and the organic layer was washed successfully with 1N NaOH, H2O, and brine, then dried (Na2SO4). Filtration and removal of the solvent afforded a solid. The solid was dissolved in hot hexane/EtOAc and the resulting solution was cooled to 0° C., filtered and stripped to give a residue which was chromatographed (Flash, Merck SiO2, 20% EtOAc in hexane). 4-(4-fluorophenyl)-2-methyl-6-phenyl-3-pyridinecarboxaldehyde was obtained as a white solid (458 mg, 83%). Analytically pure material was obtained by recrystallization from hot hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506219
Source datasetuspto-grants-1996_04
ORD IDord-8e1804a9c54a40d69b3eef425118ecc9
Source noteuspto-grants-1996_04