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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1027369Generated: October 25, 2026

Hydrochloric Acid → 2-(2,6-Diethyl-4-methylphenyl)-5-([1,3]dioxolan-2-ylmethyl)cyclohexane-1,3-dione

https://huagongshe.com/reaction/1027369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantIodine, ion (I1+)HCID 3715291—
Reactant(2,6-Diethyl-4-methylphenyl)boronic acidHCID 57437319—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
Product2-(2,6-Diethyl-4-methylphenyl)-5-([1,3]dioxolan-2-ylmethyl)cyclohexane-1,3-dioneHCID 66725107—

Reaction Conditions

Temperature55 °C

Reaction Steps

The iodonium ylide (477 mg, 1.19 mmol) prepared in Step 3a is added to a mixture of 2,6-diethyl-4-methylphenylboronic acid (343 mg, 1.79 mmol), tetrabutylammonium bromide (385 mg, 1.19 mmol), lithium hydroxide monohydrate (151 mg, 3.57 mmol) and palladium (II) acetate (13 mgs) in a mixture of 1,2-dimethoxyethane (10.8 ml) and water (2.7 ml) and the reaction mixture is heated at 55° C. for 5 hours. The reaction is then cooled, dilute aqueous hydrochloric acid is added, and the mixture is extracted with ethyl acetate. The organic extracts are combined, washed with water, dried over anhydrous magnesium sulfate, filtered and the filtrate is concentrated in vacuo. The residue is purified by column chromatography on silica gel to give 2-(2,6-diethyl-4-methylphenyl)-5-([1,3]dioxolan-2-ylmethyl)cyclohexane-1,3-dione

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08735322B2
Source datasetuspto-grants-2014_05
ORD IDord-092fb6cee83243338803759582fbd833
Source noteuspto-grants-2014_05