Реакция #513758

Уравнение реакции

pyridinium chlorochromate

α-terpineol

m-chloroperbenzoic acid

ethylene dichloride

→

1,3,3-trimethyl-2-oxabicyclo [2,2,2]octan-6-one

Растворители

methylene chloride

Условия реакции

Обработка

1. 1
   workup.ADDITIONA mixture of 3.08 g
2. 2
   Промывкаwashed with aqueous sodium bisulfite and sodium bicarbonate solutions
3. 3
   ДругоеThe solvent is removed in vacuo
4. 4
   workup.ADDITIONthe resulting oil is treated in situ with 2.94 g
5. 5
   workup.ADDITIONAfter addition of 200 ml
6. 6
   Фильтрацияdiethyl ether, the mixture is filtered through celite
7. 7
   Другоеthe solvent evaporated

Методика

A mixture of 3.08 g. (0.02 mole) α-terpineol and 4.45 g. (0.022 mole) of 85 percent m-chloroperbenzoic acid in 70 ml. of ethylene dichloride is refluxed under nitrogen for 20 hours, then cooled to room temperature and washed with aqueous sodium bisulfite and sodium bicarbonate solutions. The solvent is removed in vacuo and the resulting oil is treated in situ with 2.94 g. (0.0136 mole) pyridinium chlorochromate. The resulting mixture is stirred under nitrogen in 35 ml. of methylene chloride at ambient temperatures for 2.5 hours. After addition of 200 ml. diethyl ether, the mixture is filtered through celite and the solvent evaporated to give, on steam distillation, 1,3,3-trimethyl-2-oxabicyclo [2,2,2]octan-6-one; m.p. 50° to 52° C.

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