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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2111053Generated: October 25, 2026

Phloroglucinol → 1,3,5-Tris(vinyloxy)benzene

https://huagongshe.com/reaction/2111053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhloroglucinolHCID 359—
ReactantVinyl AcetateHCID 7904—
ReactantSodium CarbonateHCID 10340—
Reactant1-Hydroxy-3,5-bis(vinyloxy)benzeneHCID 22935762—
Reactant1,3-Dihydroxy-5-vinyloxybenzeneHCID 22935814—
SolventTolueneHCID 1140—
Product1,3,5-Tris(vinyloxy)benzeneHCID 11820226—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of di-μ-chlorobis(1,5-cyclooctadiene)diiridium(I) [Ir(cod)Cl]2 (67 mg, 0.1 mmol) and sodium carbonate (640 mg, 6 mmol) in toluene (5 ml) were added 1,3,5-trihydroxybenzene (5 mmol) and vinyl acetate (2.15 g, 25 mmol), followed by stirring at 100° C. in an atmosphere of argon gas for 6 hours. The reaction mixture was analyzed by gas chromatography to find that 1,3-dihydroxy-5-vinyloxybenzene, 1-hydroxy-3,5-bis(vinyloxy)benzene, and 1,3,5-tris(vinyloxy)benzene were formed in yields of 5%, 4%, and 18%, respectively, with a conversion from 1,3,5-trihydroxybenzene of 29%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07518021B2
Source datasetuspto-grants-2009_04
ORD IDord-2a8a427d2684410f82b3555cd7176b78
Source noteuspto-grants-2009_04