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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986462Generated: October 30, 2026

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

https://huagongshe.com/reaction/986462

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 numberUS04713387
Source datasetuspto-grants-1987_12
ORD IDord-4a881a7a0f704ea9afb52c34c0ecec61
Source noteuspto-grants-1987_12