반응 #168974

ord-146f0eaa7c2f4e03bf4d6a538b7fdc8b

반응 방정식

[Cl-].[NH4+]
NH4Cl
COc1cccc(C=NC2CCCCC2)c1
cyclohexyl-(3-methoxy-benzylidene)-amine
C1CCOC1
THF
CCI
Iodoethane
Cl
HCl
C1CCOC1
THF
CC1(C)CCCC(C)(C)N1
2,2,6,6-tetramethylpiperidine
[Li][CH2]CCC
n-butyllithium
C1CCOC1
THF
CCc1c(C=O)cccc1OC
2-ethyl-3-methoxy benzaldehyde
수율 63.0%

용매

반응 조건

온도
-15°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도drop-wise maintaining the internal temperature below −10° C
  2. 2
    온도After 1 h the solution was cooled to −78° C
  3. 3
    온도to warm to rt over 45 min
  4. 4
    추출extracted with Et2O
  5. 5
    세척The combined organics were washed with H2O
  6. 6
    세척washed with brine
  7. 7
    건조dried over MgSO4
  8. 8
    여과filtered
  9. 9
    농축concentrated in vacuo
  10. 10
    기타to give a crude imine as an oil
  11. 11
    온도After 2 the solution was cooled
  12. 12
    추출the mixture was extracted with ethyl acetate
  13. 13
    세척The combined organics were washed with H2O
  14. 14
    세척washed with brine
  15. 15
    건조dried over Na2SO4
  16. 16
    여과filtered
  17. 17
    농축concentrated in vacuo
  18. 18
    기타to give a crude oil
  19. 19
    기타Purification via flash chromatography (98:2 hexane/ethyl acetate)

실험 절차

To a solution of 2,2,6,6-tetramethylpiperidine (4.67 g, 33 mmol) in 75 ml THF at −15° C. was added n-butyllithium (12.6 ml, 32 mmol, 2.5 in hexanes) drop-wise maintaining the internal temperature below −10° C. After 15 min a solution of cyclohexyl-(3-methoxy-benzylidene)-amine (3.259 g, 15.0 mmol) in 5.0 ml THF was added and the solution was allowed to stir at −15° C. After 1 h the solution was cooled to −78° C. Iodoethane (11.9 ml, 150 mmol) was added in one portion and the solution was allowed to warm to rt over 45 min, poured into 10% NH4Cl, and extracted with Et2O. The combined organics were washed with H2O, washed with brine, dried over MgSO4, filtered and concentrated in vacuo to give a crude imine as an oil. The oil was taken up in 90 ml of THF and HCl (22 ml, 89 mmol, 4.0 M) and warmed to reflux. After 2 the solution was cooled. H2O was added and the mixture was extracted with ethyl acetate. The combined organics were washed with H2O, washed with brine, dried over Na2SO4, filtered and concentrated in vacuo to give a crude oil. Purification via flash chromatography (98:2 hexane/ethyl acetate) gave 2-ethyl-3-methoxy benzaldehyde (1.543 g, 63%, 2 steps) as a clear oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08846705B2uspto-grants-2014_09