تفاعل #66652

ord-ba49046829ca48738843f8ff099ce829

المذيبات

ظروف التفاعل

درجة الحرارة
-15°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةdrop-wise maintaining the internal temperature below −10° C
  2. 2
    درجة الحرارةAfter 1 h the solution was cooled to −78° C
  3. 3
    درجة الحرارةto warm to rt over 45 min
  4. 4
    استخلاصextracted with Et2O
  5. 5
    غسيلThe combined organics were washed with H2O
  6. 6
    غسيلwashed with brine
  7. 7
    تجفيفdried over MgSO4
  8. 8
    ترشيحfiltered
  9. 9
    تركيزconcentrated in vacuo
  10. 10
    أخرىto give a crude imine as an oil
  11. 11
    درجة الحرارةAfter 2 the solution was cooled
  12. 12
    استخلاصthe mixture was extracted with ethyl acetate
  13. 13
    غسيلThe combined organics were washed with H2O
  14. 14
    غسيلwashed with brine
  15. 15
    تجفيفdried over Na2SO4
  16. 16
    ترشيحfiltered
  17. 17
    تركيزconcentrated in vacuo
  18. 18
    أخرىto give a crude oil
  19. 19
    أخرىPurification via flash chromatography (98:2 hexane/ethyl acetate)

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524725B2uspto-grants-2013_09