تفاعل #9902

ord-1031d7c9f29c406cb2da0b969215688a

معادلة التفاعل

COC(=O)CCCCC=C1CCCC1
6-cyclopentylidene-hexanoic acid methyl ester
CC(C)[CH2][AlH][CH2]C(C)C
DIBAL-H
OCCCCCC=C1CCCC1
6-cyclopentylidene-hexan-1-ol
المردود 104.1%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe reaction was quenched by MeOH (10 mL)
  2. 2
    workup.ADDITIONSaturated aqueous sodium potassium tartrate (80 mL) was added to the reaction mixture
  3. 3
    أخرىthe organic layer was separated
  4. 4
    استخلاصthe aqueous phase was extracted with ether
  5. 5
    غسيلThe combined organic layers were washed with water and brine
  6. 6
    أخرىdried
  7. 7
    أخرىEvaporation of the solvent

الإجراء التجريبي

To a stirred solution of 6-cyclopentylidene-hexanoic acid methyl ester (2.77 g, 14.1 mmol) in toluene (130 mL) was added DIBAL-H (35.3 mL, 1 M solution in hexane, 35.3 mmol) dropwise at 0° C. under N2. After sting at 0° C. for 30 min, the reaction was quenched by MeOH (10 mL). Saturated aqueous sodium potassium tartrate (80 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 6-cyclopentylidene-hexan-1-ol (2.47 g, 98%) as a colorless oil: 1H NMR (300 MHz, CDCl3) δ 5.24 (1H, m), 3.63 (2H, t, J=6.6 Hz), 2.21 (4H, m), 1.97 (2H, m), 1.50–1.70 (6H, m), 1.34 (2H, m); 13C NMR (75 MHz, CDCl3) δ 143.28, 120.08, 63.22, 33.82, 33.00, 29.81, 29.75, 28.87, 26.72, 26.63, 25.73.

المصدر

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