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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165449Generated: October 31, 2026

Toluene → HCID 53941966, compound

https://huagongshe.com/reaction/2165449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant2-AllylphenolHCID 15624—
Reactant2,4'-DifluorobenzophenoneHCID 67651—
ProductHCID 53941966HCID 53941966—

Reaction Conditions

Temperature160 °C

Reaction Steps

o-Allylphenol (245.6 g), 2,4'-difluorobenzophenone (200 g), potassium carbonate (187.4 g), dry N-methylpyrrolidone (700 ml) and toluene (250 ml) are placed in a 3-necked 2500 ml flask fitted with a stirrer, reflex condensor and thermometer and the mixture is heated under nitrogen to a temperature of 160° C. and stirred for 8 hours. Water and toluene are separated via a Dean Stark trap and finally after 8 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 (1100 ml) is added while stirring. After phase separation the aqueous layer is washed with toluene (200 ml) and the combined toluene layers are washed 4 times with water (400 ml). The toluene phase is dried over sodium sulphate and toluene distilled off by use of a rotary evaporator finally in vacuum leaving 2,4'-bis[o-(1-propenyl)phenoxy]benzophenone as a light yellow melt. The yield is 396 g. The product has a melt viscosity of 350 mPa.s at 70° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04939305
Source datasetuspto-grants-1990_07
ORD IDord-873decb9631445499215810bdb9e30bb
Source noteuspto-grants-1990_07