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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569177Generated: October 27, 2026

Methyl Acetate → 3-[p-(3-Acetoxy-1-chloro-2-methylpropyl)benzyl]pyridine

https://huagongshe.com/reaction/569177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcetateHCID 6584—
ReactantThionyl ChlorideHCID 24386—
ReactantSodium BicarbonateHCID 516892—
Reactant3-[p-(3-Acetoxy-1-hydroxy-2-methylpropyl)benzyl]pyridineHCID 20148636—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-[p-(3-Acetoxy-1-chloro-2-methylpropyl)benzyl]pyridineHCID 1374552886%

Reaction Steps

In 4.6 ml of methylene chloride was dissolved 910 mg of 3-[p-(3-acetoxy-1-hydroxy-2-methylpropyl)benzyl]pyridine, and to the resulting solution was added 0.48 ml of thionyl chloride with ice-cooling, after which the resulting mixture was subjected to reaction at the same temperature for one hour. The solvent and the excessive thionyl chloride were removed by distillation under reduced pressure, and to the residue thus obtained were added 10 ml of methyl acetate and 10 ml of water, after which the resulting mixture was neutralized with sodium hydrogencarbonate. The organic layer was separated, washed with 5 ml of water, and then dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, and the residue thus obtained was purified by a column chromatography [Wako Silica Gel C-200, eluant: benzene:ethyl acetate (5:1 by volume)] to obtain 740 mg (yield 86.0%) of colorless, oily 3-[p-(3-acetoxy-1-chloro-2-methylpropyl)benzyl]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731370
Source datasetuspto-grants-1988_03
ORD IDord-7962bbd87b844780b3401364221aeb4e
Source noteuspto-grants-1988_03