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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 414149Generated: October 26, 2026

Potassium Carbonate → 4-[o-(1-Propenyl)phenoxy]benzophenone

https://huagongshe.com/reaction/414149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant2-AllylphenolHCID 15624—
Reactant4-FluorobenzophenoneHCID 67663—
SolventTolueneHCID 1140—
Product4-[o-(1-Propenyl)phenoxy]benzophenoneHCID 54415597—

Reaction Conditions

Temperature100 °C

Reaction Steps

o-Allylphenol (33.5 g), 4-fluorobenzophenone (50.05 g), potassium carbonate (24.20 g), dry N-methylpyrrolidone (160 ml) and toluene (60 ml) are placed in a 3-necked 500 ml flask fitted with a stirrer, reflex condensor and thermometer and the mixture is heated under nitrogen to a temperature between 155°-160° C. and stirred for 3 hours. Water and toluene are separated via a Dean Stark trap and finally after 3 hours the reaction mixture reaches a temperature of 160° C. The mixture is cooled to 100° C. and a 1:1 mixture of toluene/water (400 ml) is added while stirring. After phase separation the aqueous layer is washed with toluene (50 ml) and the combined toluene layers are washed 4 times with water (150 ml). The toluene phase is dried over sodium sulphate and toluene distilled off by use of a rotary evaporator finally in vacuum leaving 4-[o-(1-propenyl)phenoxy]benzophenone as a light yellow melt. The yield is 73 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04789704
Source datasetuspto-grants-1988_12
ORD IDord-33fb45e1eee9447baa9e133e19e2a1bc
Source noteuspto-grants-1988_12