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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946925Generated: October 27, 2026

Water → 2-(3-Isopropenyl-phenyl)-[1,3]dioxolane

https://huagongshe.com/reaction/1946925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant2-(3-Bromophenyl)-1,3-dioxolaneHCID 87306—
Reactant4,4,5,5-Tetramethyl-2-(prop-1-en-2-yl)-1,3,2-dioxaborolaneHCID 10997426—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(3-Isopropenyl-phenyl)-[1,3]dioxolaneHCID 6664977468%

Reaction Conditions

Temperature90 °C

Reaction Steps

A degassed solution of 2-(3-bromo-phenyl)-[1,3]dioxolane (3.46 ml, 22.6 mmol) in dimethoxyethane (60 ml) was added into a tube which has been charged with a mixture of 2-isopropenyl-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (3.8 g, 22.6 mmol) and an aqueous solution of sodium carbonate (1M, 20 ml); tetrakis(triphenylphosphine)palladium(0) (0.266 g) is then added, the tube is sealed and heated to 90° C. overnight. After cooling of the reaction mixture, water (20 ml) was added, the aqueous layer separated and extracted with dichloromethane (3×20 ml). The combined organic layers were dried over sodium sulphate and evaporated. The crude product was purified by chromatography on silica gel using cyclohexane as the eluent. There were obtained 2.85 g (68% of theory) of the 2-(3-isopropenyl-phenyl)-[1,3]dioxolane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399459B2
Source datasetuspto-grants-2013_03
ORD IDord-ff5f72dac3ad421e87041024a73476d1
Source noteuspto-grants-2013_03