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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073463Generated: October 27, 2026

4,4'-Difluorobenzophenone → 4,4'-Bis[o-(1-propenyl)phenoxy]benzophenone 4-[o-(1-propenyl)phenoxy]benzophenone

https://huagongshe.com/reaction/2073463

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4'-DifluorobenzophenoneHCID 9582—
ReactantPotassium CarbonateHCID 11430—
Reactant2-AllylphenolHCID 15624—
Reactant4-FluorobenzophenoneHCID 67663—
SolventTolueneHCID 1140—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4,4'-Bis[o-(1-propenyl)phenoxy]benzophenone 4-[o-(1-propenyl)phenoxy]benzophenoneHCID 86742606—

Reaction Conditions

Temperature100 °C

Reaction Steps

o-Allylphenol (52.2 g), 4,4'-difluorobenzophenone (35 g), 4-fluorobenzophenone (13.8 g), potassium carbonate (37.75 g), dry N-methylpyrrolidone (200 ml) and toluene (75 ml) are placed in a 3-necked 1500 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 (100 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 a 4,4'-bis-[o-(1-propenyl)phenoxy]benzophenone/4-[o-(1-propenyl)-phenoxy]benzophenone mixture as a light yellow melt. The yield is 89 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04917954
Source datasetuspto-grants-1990_04
ORD IDord-2e04ea7160374c4594002632a786e05f
Source noteuspto-grants-1990_04