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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623343Generated: October 30, 2026

Acetone → 3,4-Diallylbenzene-1,2-diol

https://huagongshe.com/reaction/623343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantCatecholHCID 289—
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Product3,4-Diallylbenzene-1,2-diolHCID 13158325—

Reaction Conditions

Temperature177.5 °C

Reaction Steps

To a solution of pyrocatechol (Compound A) (1 g, 0.009 mol) and dry acetone (10 mL) was added dry K2CO3 (2.646 g, 0.0189 mol) in portions for 30 minutes. The stirring was continued for another hour. Allyl bromide (1.6 mL, 0.0189 mol) was added to the mixture for 30 minutes and the mixture was refluxed for 5 hours. After completion of the reaction, the solid was filtered and filtrate was concentrated and extracted with chloroform (3×50 mL), washed with brine (1×50 mL), dried over anhydrous sodium sulfate and solvent was removed under reduced pressure. The crude material was heated at 175-180° C. for 2 hours. The reaction mixture was purified by column chromatography (silica gel: 60-120 mesh) using petroleum ether with increasing concentration of chloroform. Elution of 60% and 75% chloroform in petroleum ether yielded pure compounds corresponding to Compound No. 2 and Compound No. 3 as liquids respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09302967B2
Source datasetuspto-grants-2016_04
ORD IDord-912cce266b374c0486508762668d0a39
Source noteuspto-grants-2016_04