반응 #1552077

ord-495092a68138441caca4e1b3583c7c21

반응 방정식

CC(C)CC1=CCC(C)(C=O)CC1
4-Isobutyl-1-methylcyclohex-3-enecarbaldehyde
[Br-].[CH3][Mg+]
MeMgBr
CC(C)CC1=CCC(C)(C(C)O)CC1
colorless oil
수율 89.9%
CC(C)CC1=CCC(C)(C(C)O)CC1
1-(4-Isobutyl-1-methylcyclohex-3-enyl)ethanol
수율 89.9%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타An ice-bath was used
  2. 2
    기타the temperature below 20° C.
  3. 3
    workup.ADDITIONwas added over 30 min
  4. 4
    기타The ice-bath was removed
  5. 5
    workup.STIRRINGthe reaction stirred for a further 30 min
  6. 6
    workup.ADDITIONbefore being poured slowly
  7. 7
    기타The phases were separated
  8. 8
    세척the upper organic phase washed twice with brine (2×100 ml)
  9. 9
    건조dried (MgSO4)
  10. 10
    농축concentrated in vacuo

실험 절차

4-Isobutyl-1-methylcyclohex-3-enecarbaldehyde 3a (20 g, 111 mmol) was dissolved in diethyl ether (120 ml) and the solution stirred under nitrogen. An ice-bath was used to keep the temperature below 20° C. while MeMgBr (3M, 48 ml, 144 mmol) was added over 30 min. The ice-bath was removed and the reaction stirred for a further 30 min before being poured slowly, and under nitrogen, onto 2M HCl (50 ml). The phases were separated and the upper organic phase washed twice with brine (2×100 ml), dried (MgSO4) and concentrated in vacuo to give 19.6 g of a colorless oil. The product was purified by distillation (0.1 mbar, 90° C.) to give 4c as a 4:5 mixture of diastereomers containing 6.5% of a third isomer (14 g, 52% yield, colourless oil, 95% pure).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08999914B2uspto-grants-2015_04