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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742775Generated: October 25, 2026

Epichlorohydrin → 2-[(4-Benzoylphenoxy)methyl]oxirane

https://huagongshe.com/reaction/1742775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
Reactant4-HydroxybenzophenoneHCID 14347—
ReactantSodium HydroxideHCID 14798—
Product2-[(4-Benzoylphenoxy)methyl]oxiraneHCID 35281683%

Reaction Conditions

Temperature100 °C

Reaction Steps

1 g of 4-hydroxy benzophenone and 4.668 g of epichlorohydrin (0.025 mol) were dissolved, 20.5 mg of sodium hydroxide was added, and the reaction system was heated to 100° C. and then cooled to 95° C. Furthermore 201.4 mg of sodium hydroxide was added, and additional heating and agitation was carried out for 3 hours. The system was cooled to the room temperature, and salt was removed by filtering. The obtained filtrate was condensed under reduced pressure condition, and purified according to the silica gel chromatography to obtain 1.0 g of solid state 4-glycidyloxy benzophenone (Yield: 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05342610
Source datasetuspto-grants-1994_08
ORD IDord-e85f38e65d7646519f71c006d78eed22
Source noteuspto-grants-1994_08