تفاعل #1797505
ord-08294551164d48f9963c6aecd27a7540
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
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المعالجة
- 1أخرىthe phases were separated
- 2استخلاصThe aqueous phase was extracted with tert.-butyl methyl ether (500 ml)
- 3غسيلThe combined organic phases were washed with water, concentrated KHCO3 solution, concentrated NaCl solution
- 4تجفيفdried over MgSO4
- 5أخرىafter the removal of the solvent
- 6workup.DISTILLATIONwas distilled over a small Vigreux-column
الإجراء التجريبي
860 g 6-Methoxy-6-methyl-2-octanone, 4 l tert.-butyl methyl ether and 648 g methyl chloroacetate were cooled to 0° C. under a blanket of nitrogen. Under further cooling, 350 g sodium methoxide was added in 6 portions over 20 minutes. The mixture was then stirred at room temperature till no more consumption of the ketone was observed (GC). After cooling to 0° C., 1 l 5% acetic acid (w/w) was added and the phases were separated. The aqueous phase was extracted with tert.-butyl methyl ether (500 ml). The combined organic phases were washed with water, concentrated KHCO3 solution, concentrated NaCl solution and dried over MgSO4. The yellow oil which remained after the removal of the solvent was distilled over a small Vigreux-column to give 823 g of 3-(4-methoxy-4-methyl-hexyl)-3-methyl-oxirane-2-carboxylic acid methyl ester (mixture of isomers, boiling point: 115°-128°/0.3 Torr=0.399 mbar).