تفاعل #3860

ord-d08bf726ee614cf79e621b0c1f4b7772

معادلة التفاعل

O=C([O-])[O-]
carbonate
O=C([O-])[O-].[K+].[K+]
potassium carbonate
C1COCCO1
1,4-dioxane
CC/C=C\C=C/CCCCCCCCCC=O
(Z,Z)-11,13-hexadecadienal
C=CCCCCCCCCC/C=C\C=C/CC
(Z,Z)-1,12,14-heptadecatriene

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas prepared in a 100 ml round bottomed flask
  2. 2
    أخرىequipped with a magnetic stirrer
  3. 3
    درجة الحرارةthermometer and reflux condenser
  4. 4
    درجة الحرارةThe mixture was heated
  5. 5
    درجة الحرارةto reflux at 105°-110°
  6. 6
    أخرىwere withdrawn periodically
  7. 7
    أخرىpartitioned between 1 ml of H2O and 1 ml of hexane
  8. 8
    أخرىat 1.1 and 2.2 and 17 hr
  9. 9
    workup.ADDITIONMore potassium carbonate (1.7 g) was added at 212 hr
  10. 10
    أخرىthe reaction to completion
  11. 11
    درجة الحرارةThe reaction mixture was cooled
  12. 12
    استخلاصextracted 3 times with 25 ml of hexane
  13. 13
    استخلاصthe organic layer was extracted with water
  14. 14
    أخرىdried
  15. 15
    أخرىthe solvent removed

الإجراء التجريبي

(Z,Z)-1,12,14-heptadecatriene (TRIENE) was synthesized conveniently from Wittig Salt and aldehyde in aqueous dioxidepotassium carbonate heterogeneous medium (Lechat 1982). A mixture of 3.57 g (0.01 mol) of methyl triphenylphosphonium bromide (Alfa Inorganics), 1.7 g (0.14 mol) of potassium carbonate, 10 ml of 1,4-dioxane, 0.15 ml of water and 2.36 g (0.01 mol) of (Z,Z)-11,13-hexadecadienal (AL. Albany International) was prepared in a 100 ml round bottomed flask equipped with a magnetic stirrer, thermometer and reflux condenser. The mixture was heated to reflux at 105°-110° with stirring while aliquots of 15 ul were withdrawn periodically and partitioned between 1 ml of H2O and 1 ml of hexane. Analysis by gas-liquid chromatography, showed 66, 70 and 99% triolefin and 30%, 26% and 1% starting aldehyde at 1.1 and 2.2 and 17 hr, respectively. More potassium carbonate (1.7 g) was added at 212 hr to drive the reaction to completion. The reaction mixture was cooled and extracted 3 times with 25 ml of hexane, then the organic layer was extracted with water, dried and the solvent removed to leave 1.8 g of yellow oil and a few crystals of triphenylphosphine oxide. The oil was taken up in hexane and passed through a 1×45 cm column of silica gel (60-200 mesh, Baker) with hexane, to yield 1.7 g (73% yield) of clear oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04722839uspto-grants-1988_02