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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075855Generated: October 30, 2026

Epichlorohydrin → 1,2-Epoxy-3-[3-(2-pyridylmethyl)phenoxy]propane

https://huagongshe.com/reaction/1075855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
Reactant3-[(Pyridin-2-yl)methyl]phenolHCID 21541318—
SolventMethanolHCID 887—
Product1,2-Epoxy-3-[3-(2-pyridylmethyl)phenoxy]propaneHCID 1291985262.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

19 g of epichlorohydrin is added to a mixture of 18.5 g of 3-(2-pyridylmethyl)phenol, 4.2 g of sodium hydroxide and 200 ml of methanol, and the resulting mixture is stirred at about 50°C for 3 hours. The methanol is then removed, water is added to the residue, and the aqueous solution is extracted with 200 ml of benzene. The benzene layer is washed with 5% sodium hydroxide and with water, and dried over anhydrous magnesium sulfate. The benzene is removed to give 15.0 g of 1,2-epoxy-3-[3-(2-pyridylmethyl)-phenoxy] propane as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954776
Source datasetuspto-grants-1976_05
ORD IDord-96f42c65db9e4ce5a0987d605fb71031
Source noteuspto-grants-1976_05