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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986458Generated: October 29, 2026

Hydrochloric Acid → 3-[p-[1-Chloro-3-(2-hydroxyethyl)oxy-2-methylpropyl]benzyl]pyridine

https://huagongshe.com/reaction/986458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
Reactant3-[p-[1-Hydroxy-3-(2-hydroxyethyl)oxy-2-methylpropyl]benzyl]pyridineHCID 20148604—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product3-[p-[1-Chloro-3-(2-hydroxyethyl)oxy-2-methylpropyl]benzyl]pyridineHCID 1374552598%

Reaction Steps

In 13.7 ml of ethanol was dissolved 2.74 g of 3-[p-[1-hydroxy-3-(2-hydroxyethyl)oxy-2-methylpropyl]benzyl]pyridine, and the resulting solution was saturated with hydrogen chloride with ice-cooling, after which the solution was subjected to reaction at room temperature for 2 hours. The solvent was removed by distillation under reduced pressure, and to the residue thus obtained were added 10 ml of water and 20 ml of ethyl acetate, after which the pH of the resulting mixture was adjusted to 7.0 with sodium hydrogencarbonate. The organic layer was separated, washed with 10 ml of water, and then dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure to obtain 2.85 g (yield 98%) of colorless, oily 3-[p-[1-chloro-3-(2-hydroxyethyl)oxy-2-methylpropyl]benzyl]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04713387
Source datasetuspto-grants-1987_12
ORD IDord-7fcbd51b28954203b2faf05f24f6059d
Source noteuspto-grants-1987_12