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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569166Generated: October 26, 2026

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

https://huagongshe.com/reaction/569166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium ChlorideHCID 5234—
Reactant3-[p-(3-Chloro-2-methylpropionyl)benzyl]pyridineHCID 13745520—
ReactantHCID 178418435HCID 178418435—
SolventEthanolHCID 702—
Product3-[p-(3-Chloro-1-hydroxy-2-methylpropyl)benzyl]pyridineHCID 2014861599%

Reaction Steps

In 17 ml of ethanol was dissolved 2.28 g of 3-[p-(3-chloro-2-methylpropionyl)benzyl]pyridine, and to the resulting solution was added 0.3 g of sodium boron hydride in small portions with ice-cooling, after which the resulting mixture was subjected to reaction at the same temperature for one hour. To the reaction mixture were added successively 0.54 ml of acetic acid and 30 ml of a saturated aqueous sodium chloride solution, and the resulting mixture was extracted with two 20-ml portions of ethyl acetate. The extracts were combined, washed with 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: chloroform:ethyl acetate (1:1 by volume)] to obtain 2.29 g (yield 99.0%) of colorless, oily 3-[p-(3-chloro-1-hydroxy-2-methylpropyl)benzyl]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731370
Source datasetuspto-grants-1988_03
ORD IDord-f565642fca0246ba9bd7ed9f2a6a2a2a
Source noteuspto-grants-1988_03