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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1493961Generated: October 25, 2026

Pyridine → 1,2-Propanediol, 3-((o-benzyloxy)phenoxy)-

https://huagongshe.com/reaction/1493961

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantGlycidolHCID 11164—
Reactant2-BenzyloxyphenolHCID 80459—
SolventEthanolHCID 702—
Product1,2-Propanediol, 3-((o-benzyloxy)phenoxy)-HCID 302205273%

Reaction Steps

A solution of 49.6 g (0.248 mole) of 2-benzyloxyphenol, 22.2 g (0.3 mole) of glycidol, 2 ml of pyridine and 150 ml of absolute ethanol was heated at reflux overnight. The dark solution was concentrated to give an oil which gradually crystallized. The solid was purified by column chromatography on 1.2 kg of silica gel eluted with 0-25% acetone in benzene. Appropriate fractions were combined and concentrated to yield 49.5 g (73%) of the title compound as a white solid, mp 84°-85° C. (carbon tetrachloride) (lit.1 mp 81°-82.5° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025031
Source datasetuspto-grants-1991_06
ORD IDord-e7004eaaac334d3085ee7566a34da6b0
Source noteuspto-grants-1991_06