تفاعل #9915

ord-6d7be9b2d98a4dcd85a633f7f75d4960

معادلة التفاعل

COC(=O)CCCCC=C(C)C
7-methyl-oct-6-enoic acid methyl ester
CC(C)[CH2][AlH][CH2]C(C)C
DIBAL-H
CC(C)=CCCCCCO
7-methyl-oct-6-en-1-ol
المردود 98.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

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

المعالجة

  1. 1
    أخرىthe reaction was quenched by MeOH (12 mL)
  2. 2
    workup.ADDITIONSaturated aqueous sodium potassium tartrate (120 mL) was added to the reaction mixture
  3. 3
    workup.STIRRINGAfter stirring for 1 h
  4. 4
    أخرىthe organic layer was separated
  5. 5
    استخلاصthe aqueous phase was extracted with ether
  6. 6
    غسيلThe combined organic layers were washed with water and brine
  7. 7
    أخرىdried
  8. 8
    أخرىEvaporation of the solvent

الإجراء التجريبي

To a stirred solution of 7-methyl-oct-6-enoic acid methyl ester (3.29 g, 19.4 mmol) in toluene (180 mL) was added DIBAL-H (48.5 mL, 1 M solution in hexane, 48.5 mmol) dropwise at 0° C. under N2. After stirring at 0° C. for 30 min, the reaction was quenched by MeOH (12 mL). Saturated aqueous sodium potassium tartrate (120 mL) was added to the reaction mixture. After stirring for 1 h, the organic layer was separated and the aqueous phase was extracted with ether. The combined organic layers were washed with water and brine and dried. Evaporation of the solvent gave 7-methyl-oct-6-en-1-ol (2.70 g, 98%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 5.11 (1H, m), 3.63 (2H, m), 1.99 (2H, m), 1.68 (3H, s), 1.59 (3H, s), 1.53 (2H, m), 1.25–1.45 (4H, m); 13C NMR (75 MHz, CDCl3) δ 131.52, 124.69, 63.25, 33.00, 29.95, 28.25, 26.02, 25.69, 17.98.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091357B2uspto-grants-2006_08