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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076461Generated: October 27, 2026

Phenol → 3-Phenoxy-3'-(m-phenoxyphenoxy)biphenyl

https://huagongshe.com/reaction/1076461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenolHCID 996—
ReactantTolueneHCID 1140—
ReactantPotassium HydroxideHCID 14797—
Reactant3-Chloro-3'-(m-phenoxyphenoxy)biphenylHCID 21536922—
CatalystCopperHCID 23978—
SolventWaterHCID 962—
SolventDiglymeHCID 8150—
Product3-Phenoxy-3'-(m-phenoxyphenoxy)biphenylHCID 21536932—

Reaction Conditions

Temperature100 °C

Reaction Steps

A 500 ml. reaction flask equipped with stirrer, condenser and Dean-Stark trap was charged with 250 g. (2.66 moles) of phenol. This was heated with stirring at 100°C. while 56 g. (1.0 mole) of potassium hydroxide was added in increments. Toluene (50 ml.) was then added to the fluld mass and water azeotroped from the system. After all toluene and water had been removed, 150 ml. of diglyme was added together with 5.0 g. (0.05 mole) of cuprous chloride and 1.0 g. of copper powder. To this mixture 20 g. (0.053 mole) of 3-chloro-3'-(m-phenoxyphenoxy)biphenyl in diglyme was added over a 30 minute period. Diglyme was distilled from the mixture which was then heated at 240° for 18 hrs. On cooling the mixture was slurried in 200 ml. of ether and salts were filtered off. The ethereal solution was washed with 25% potassium hydroxide solution, water until neutral and then dried over magnesium sulfate. The ether was removed under vacuum and the resulting oil distilled to give 13.1 g. of the desired product, bp 248°-253° /0.06 mm., nD25 1.6474.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03957666
Source datasetuspto-grants-1976_05
ORD IDord-20d65c4d6c314de682b4a446e8cb2c21
Source noteuspto-grants-1976_05