Reaktion #4243

Reaktionsgleichung

4-allyl-2,6-dimethylphenyl glycidyl ether

formic acid

hydrogen peroxide

→

4-(2,3-epoxypropyl)-2,6-dimethylphenyl glycidyl ether

Ausbeute 85.5%

Lösungsmittel

chloroform

chloroform

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigeequipped with thermometer, stirrer, cooler and drip funnel
2. 2
   Sonstigeis held at this temperature overnight
3. 3
   Waschenthe resultant solution is washed twice with 3% NaOH solution until neutral,
4. 4
   Trocknendried over sodium sulfate
5. 5
   Filtrationfiltered
6. 6
   EinengenThe filtrate is concentrated

Vorschrift

A 350 ml sulfurating flask equipped with thermometer, stirrer, cooler and drip funnel is charged with 21.8 g (0.10 mole) of 4-allyl-2,6-dimethylphenyl glycidyl ether, 10.9 g (0.24 mole) of formic acid and 135 ml of chloroform. At room temperature, 23.2 g (0.47 mole) of hydrogen peroxide are then added dropise over 4 hours. The reaction miture is held at this temperature overnight. It is subsequently taken up in chloroform and the resultant solution is washed twice with 3% NaOH solution until neutral, made peroxide-free with sodium sulfite, dried over sodium sulfate and filtered. The filtrate is concentrated, affording 20.03 g (80.50% of theory) of 4-(2,3-epoxypropyl)-2,6-dimethylphenyl glycidyl ether in the form of a low viscous resin; epoxide content 7.7 equivalents/kg (90.11% of theory).

Quelle