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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1824666Generated: October 25, 2026

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

https://huagongshe.com/reaction/1824666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantPotassium CarbonateHCID 11430—
Reactant4-HydroxybenzophenoneHCID 14347—
SolventAcetoneHCID 180—
Product2-[(4-Benzoylphenoxy)methyl]oxiraneHCID 352816—

Reaction Steps

As illustrated in FIG. 6, 100 mL of dried acetone were added to a dry, 250-mL round bottom flask, equipped with a magnetic stirrer, along with 15.05 grams of 4-hydroxybenzophenone, 32.1 grams of epichlorohydrin, and 6.2 grams of potassium carbonate. The solution was heated to reflux for 6 hours and then cooled to room temperature. The precipitated potassium chloride was filtered off, and the solution was evaporated to remove excess epichlorohydrin. The crude product was recrystallized from methanol. 1H NMR data confirmed the formation of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045366B2
Source datasetuspto-grants-2006_05
ORD IDord-11abb5634ed142ee9bd12b16b8fc0da6
Source noteuspto-grants-2006_05