تفاعل #1797505

ord-08294551164d48f9963c6aecd27a7540

معادلة التفاعل

C[O-].[Na+]
sodium methoxide
CCC(C)(CCCC(C)=O)OC
6-Methoxy-6-methyl-2-octanone
COC(C)(C)C
tert.-butyl methyl ether
COC(=O)CCl
methyl chloroacetate
CCC(C)(CCCC1(C)OC1C(=O)OC)OC
3-(4-methoxy-4-methyl-hexyl)-3-methyl-oxirane-2-carboxylic acid methyl ester
المردود 67.5%

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe phases were separated
  2. 2
    استخلاصThe aqueous phase was extracted with tert.-butyl methyl ether (500 ml)
  3. 3
    غسيلThe combined organic phases were washed with water, concentrated KHCO3 solution, concentrated NaCl solution
  4. 4
    تجفيفdried over MgSO4
  5. 5
    أخرىafter the removal of the solvent
  6. 6
    workup.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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07790668B2uspto-grants-2010_09