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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156421Generated: October 28, 2026

3,4-Dichlorobenzotrifluoride → HCID 13094093, compound

https://huagongshe.com/reaction/1156421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DichlorobenzotrifluorideHCID 9481—
ReactantPotassium HydroxideHCID 14797—
ReactantPotassiumHCID 5462222—
Reactant2-[2-[[2-(2,5-Dihydroxyphenyl)phenyl]methoxymethyl]phenyl]benzene-1,4-diolHCID 131711022—
SolventMethanolHCID 887—
ProductHCID 13094093HCID 1309409370%

Reaction Conditions

Temperature120 °C

Reaction Steps

To as flask equipped with a stirrer, thermometer, condenser and drying tube are charged 3,4-dichlorobenzotrifluoride (43 g., 0.20 mole), potassium 4-benzyloxyphenate (47.5 g., 0.20 mole-prepared from hydroquinone monobenzylether using potassium hydroxide pellets dissolved in methanol and removal of the solvent in vacuo and subsequent precipitation in ether) and dimethyl sulfoxide (400 ml.). The reaction mixture is then warmed to 120° C. and maintained at 135° C. for 3 hours, cooled, poured into water (3 liters) and extracted into hexane (500 ml., then 300 ml., then 200 ml.) and the combined hexane extracts washed again with water (200 ml.), dried with anhydrous magnesium sulfate, and the solvent removed in vacuo to give 52.6 g. (70% yield) of 4-benzyloxyphenyl 2-chloro-4-trifluoromethylphenyl ether, mp 63°-6° C., which is recrystallized from methanol to give white crystals, mp 69°-71° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04335249
Source datasetuspto-grants-1982_06
ORD IDord-dfce760f351d463eb56e6c1b34498f2d
Source noteuspto-grants-1982_06