تفاعل #2348118

ord-3ea3f627ac084da6bafffe4eb0b664e5

معادلة التفاعل

C1=C\CCCCCCC2OC2CCCCCC/1
(Z)-17-oxabicyclo[14.1.0]heptadec-8-ene
CC(=O)OO
peracetic acid
C1=C\CCCCCCC2OC2CCCCCC/1
(Z)-17-oxabicyclo[14.1.0]heptadec-8-ene
C1=C/CCCCCC/C=C/CCCCCC/1
(E,E)-1,9-cyclohexadecadiene
C1=C\CCCCCC/C=C\CCCCCC/1
(Z,Z)-1,9-cyclohexadecadiene
C1=C\CCCCCC/C=C/CCCCCC/1
(E,Z)-1,9-cyclohexadecadiene
C1=CCCCCCCC=CCCCCCC1
1,9-cyclohexadecadiene
CC(=O)[O-].[Na+]
sodium acetate
C1=C/CCCCCCC2OC2CCCCCC/1
(E)-17-oxabicyclo[14.1.0]heptadec-8-ene
C1=C/CCCCCCC2OC2CCCCCC/1
(E)-17-oxabicyclo[14.1.0]heptadec-8-ene
C1=CCCCCCCC2OC2CCCCCC1
17-oxabicyclo[14.1.0]heptadec-8-ene

ظروف التفاعل

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

المعالجة

  1. 1
    استخلاصextracted once with methylene chloride
  2. 2
    غسيلThe combined organic phases are washed with saturated NaCl solution
  3. 3
    تجفيفsubsequently dried with magnesium sulfate
  4. 4
    أخرىafter removal of the solvent 9.0 g of crude product
  5. 5
    أخرىare obtained
  6. 6
    أخرىAfter purification by chromatography with ethyl acetate/cyclohexane
  7. 7
    أخرىis obtained

الإجراء التجريبي

10 g 1,9-cyclohexadecadiene of the following composition are added to a solution of 14.1 g sodium acetate in 75 ml methylene chloride and the mixture is cooled to 0° C.: (Z,Z)-1,9-cyclohexadecadiene 18%, (E,Z)-1,9-cyclohexadecadiene 54%, (E,E)-1,9-cyclohexadecadiene 28%. 8.6 g peracetic acid (40% strength) in 15 ml methylene chloride are slowly added dropwise at this temperature and the mixture is subsequently stirred for three hours at 0° C. The reaction solution is poured on to ice-water and extracted once with methylene chloride. The combined organic phases are washed with saturated NaCl solution and subsequently dried with magnesium sulfate, and after removal of the solvent 9.0 g of crude product are obtained. After purification by chromatography with ethyl acetate/cyclohexane, a product having the following composition is obtained: (E)-17-oxabicyclo[14.1.0]heptadec-8-ene (1) 33%, (E)-17-oxabicyclo[14.1.0]heptadec-8-ene (2) 28%, (Z)-17-oxabicyclo[14.1.0]heptadec-8-ene (3) 21%, (Z)-17-oxabicyclo[14.1.0]heptadec-8-ene (4) 18%.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07846886B2uspto-grants-2010_12