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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 909683Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/909683

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl Ethyl KetoneHCID 6569—
EduktEpichlorohydrinHCID 7835—
EduktSodium HydroxideHCID 14798—
Edukt4,4'-(1,3-Adamantanediyl)diphenolHCID 4454346—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelMethyl Isobutyl KetoneHCID 7909—
Produkt1,3-Bis(4-glycidyloxyphenyl)adamantaneHCID 1870426792,9%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08017800B2
Quelldatensatzuspto-grants-2011_09
ORD IDord-9cae096d794f496f8613b97ccf200a8d
Quellennotizuspto-grants-2011_09