반응 #1552075

ord-f0c66e45f9c7415f904df9a6d9e8ad36

반응 방정식

CC(C)CC1=CCC(C=O)C(C)C1
4-Isobutyl-6-methylcyclohex-3-enecarbaldehyde
CC(C)(C)[O-].[K+]
KOtBu
CI
MeI
CC(C)CC1=CCC(C)(C=O)C(C)C1
orange oil
수율 99.4%
CC(C)CC1=CCC(C)(C=O)C(C)C1
4-Isobutyl-1,6-dimethylcyclohex-3-enecarbaldehyde
수율 99.4%

반응 조건

온도
-3°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.STIRRINGthe suspension stirred for 30 min
  2. 2
    기타to return to room temperature
  3. 3
    workup.STIRRINGAfter stirring for a further 3 h
  4. 4
    기타the reaction crude
  5. 5
    workup.ADDITIONwas poured onto brine (400 ml)
  6. 6
    workup.STIRRINGstirred for 10 min
  7. 7
    기타to separate
  8. 8
    추출The upper aqueous phase was extracted with methylene chloride (150 ml)
  9. 9
    건조dried (Na2SO4)
  10. 10
    농축concentrated in vacuo

실험 절차

4-Isobutyl-6-methylcyclohex-3-enecarbaldehyde 3b (8 g, 44 mmol) was dissolved in methylene chloride (400 ml) and cooled to −3° C. with stirring and under nitrogen. KOtBu (6.7 g, 58 mmol) and MeI (19 g, 130 mmol) were added sequentially and the suspension stirred for 30 min before being allowed to return to room temperature. After stirring for a further 3 h the reaction crude was poured onto brine (400 ml), stirred for 10 min and the phases allowed to separate. The upper aqueous phase was extracted with methylene chloride (150 ml) and the organic phases combined, dried (Na2SO4) and concentrated in vacuo to give 8.5 g of an orange oil (8.5 g). The oil was purified by flash chromatography (MTBE/hexane 1:9) and combination of pure fractions gave 3c as a 7:3 mixture of diastereomers (7 g, colorless oil, 80% yield). 1 g of the oil was distilled to give a sample for olfactory assessment. (0.52 g, colourless oil, >99% pure).

출처

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