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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712185Generated: October 25, 2026

Methyl Ethyl Ketone → 1,3-Bis(4-glycidyloxyphenyl)adamantane

https://huagongshe.com/reaction/1712185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
Reactant4,4'-(1,3-Adamantanediyl)diphenolHCID 4454346—
SolventDimethyl SulfoxideHCID 679—
SolventMethyl Isobutyl KetoneHCID 7909—
Product1,3-Bis(4-glycidyloxyphenyl)adamantaneHCID 1870426792.9%

Reaction Conditions

Temperature45 °C

Reaction Steps

In a separable flask having an inner volume of 300 ml, equipped with a reflux condenser, a stirrer, and a thermometer, were charged 20.0 g (0.06 mol) of 1,3-bis(4-hydroxyphenyl)adamantane, 46 g (0.50 mol) of epichlorohydrin, 30 mL of MIBK, and 60 mL of DMSO, and they were heated to 45° C. Then, 5.5 g (0.14 mol) of sodium hydroxide was added into this solution by small portions during a period of 1.5 hours. After completion of the addition, the reaction temperature was raised to 75° C., and the reaction was carried out for 4 hours. After the reaction was completed, the mixture was cooled to room temperature, added by 25 mL of MIBK, and washed with water until the aqueous layer became neutral. The resulting organic layer was concentrated to obtain pale yellow solids. The pale yellow solids were dissolved in 285 g of MEK, added by 3.4 g of 25% by mass of aqueous sodium hydroxide solution, and then the mixture was stirred for 2 hours under reflux. Thereafter, the solution was cooled to room temperature, and washed by water until the aqueous layer became neutral from alkaline. The water-washing was performed two more times, and then the organic layer was concentrated to obtain pale yellow solids, which was recrystallized by a mixed solvent of THF (tetrahydrofuran) and isopropyl ether to obtain 24.1 g of 1,3-bis(4-glycidyloxyphenyl)adamantane having the following formula (purity of 94% by LC (liquid chromatography), epoxy equivalent of 224).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790917B2
Source datasetuspto-grants-2010_09
ORD IDord-600bfbc63c874267a1f56223c354ce93
Source noteuspto-grants-2010_09