반응 #11311

ord-11d6b4e2d7e343d0996c130ebd1192a0

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGwas stirred for 1 hr
  2. 2
    기타to quench
  3. 3
    기타the reaction
  4. 4
    기타the organic layer was separated
  5. 5
    추출The aqueous layer was extracted with dichloromethane 3 times
  6. 6
    건조the combined organic layers were dried over magnesium sulfate
  7. 7
    여과filtered
  8. 8
    농축concentrated under vacuum
  9. 9
    기타The crude material was purified
  10. 10
    여과by filtering through a short silica gel pad with dichloromethane

실험 절차

At −78° C., 3-ethylenedioxy-1-phenylcyclohexanecarbonitrile (1.66 g, 6.83 mmol) in toluene (20 mL) was added DIBAL-H (1.0 M solution in toluene, 8.88 mL) slowly and was stirred for 1 hr. The reaction mixture was warmed up to room temperature and was added 1N HCl solution (2.60 mL) and was stirred for 1 hr. Saturated sodium bicarbonate was added to quench the reaction and the organic layer was separated. The aqueous layer was extracted with dichloromethane 3 times and the combined organic layers were dried over magnesium sulfate, filtered and concentrated under vacuum. The crude material was purified by filtering through a short silica gel pad with dichloromethane to give the title compound as a white sticky oil (1.43 g, 85% yield). 1H NMR (400 MHz, CDCl3) δ 1.32–1.40 (1H, m), 1.46–1.54 (1H, m), 1.72–1.86 (3H, m), 2.08 (1H, d, J=16 Hz), 2.59–2.67 (2H, m), 3.94–4.07 (4H, m), 7.15–7.36 (5H, m), 9.36 (1H, d, J=4 Hz).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07098203B2uspto-grants-2006_08