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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986461Generated: October 27, 2026

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

https://huagongshe.com/reaction/986461

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 numberUS04713387
Source datasetuspto-grants-1987_12
ORD IDord-e849927b6a49410bb65a35c1f6a5c036
Source noteuspto-grants-1987_12