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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569178Generated: October 29, 2026

Acetic Acid → 3-[p-(1-Chloro-3-hydroxy-2-methylpropyl)benzyl]pyridine

https://huagongshe.com/reaction/569178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium MethoxideHCID 10942334—
Reactant3-[p-(3-Acetoxy-1-chloro-2-methylpropyl)benzyl]pyridineHCID 13745528—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product3-[p-(1-Chloro-3-hydroxy-2-methylpropyl)benzyl]pyridineHCID 1374552962.3%

Reaction Steps

In 10 ml of methanol was dissolved 740 mg of 3-[p-(3-acetoxy-1-chloro-2-methylpropyl)benzyl]pyridine, and to the resulting solution was added 40 mg of sodium methoxide with ice-cooling, after which the resulting mixture was subjected to reaction at room temperature for 30 minutes. To the reaction mixture was added 0.1 ml of acetic acid, and the solvent was removed by distillation under reduced pressure, after which the residue thus obtained was dissolved in 10 ml of ethyl acetate. The resulting solution was washed with 5 ml of water and then dried over anhydrous magnesium sulfate. The residue thus obtained was purified by a column chromatography [Wako Silica Gel C-200, eluant: benzene:ethyl acetate (1:1 by volume)] to obtain 400 mg (yield 62.3%) of colorless, oily 3-[p-(1-chloro-3-hydroxy-2-methylpropyl)benzyl]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731370
Source datasetuspto-grants-1988_03
ORD IDord-01dda6a01dee44e8aaf3271c4df0bec6
Source noteuspto-grants-1988_03