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Hydrochloric Acid → 2-Ethyl-3-methoxybenzaldehyde

HRID 38374
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HRID 38374 반응식
CC1(C)CCCC(C)(C)N1.[CH2:11]([Li])[CH2:12][CH2:13][CH3:14].C1(N=C[C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([O:30]C)C=2)CCCCC1.ICC.[NH4+].[Cl-].Cl.C1C[O:41][CH2:40]C1>O>[CH2:13]([C:12]1[C:11]([O:41][CH3:40])=[CH:24][CH:29]=[CH:28][C:27]=1[CH:26]=[O:30])[CH3:14]
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참가 물질

9

반응물 7

HCID 313Hydrochloric AcidHCID 6340IodoethaneHCID 8028Tetrahydrofuran3회HCID 130352,2,6,6-TetramethylpiperidineHCID 25517Ammonium ChlorideHCID 11672973N-(3-Methoxybenzylidene)cyclohexanamineHCID 178418339Butyllithium

생성물 1

HCID 595986312-Ethyl-3-methoxybenzaldehyde수율 63%

시약·촉매·용매 1

HCID 962Water용매

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온도
-15 °C

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.

후처리

  1. temperaturedrop-wise maintaining the internal temperature below −10° C
  2. temperatureAfter 1 h the solution was cooled to −78° C
  3. temperatureto warm to rt over 45 min
  4. extractionextracted with Et2O
  5. washThe combined organics were washed with H2O
  6. washwashed with brine
  7. dry with materialdried over MgSO4
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo
  10. customto give a crude imine as an oil
  11. temperatureAfter 2 the solution was cooled
  12. extractionthe mixture was extracted with ethyl acetate
  13. washThe combined organics were washed with H2O
  14. washwashed with brine
  15. dry with materialdried over Na2SO4
  16. filtrationfiltered
  17. concentrationconcentrated in vacuo
  18. customto give a crude oil
  19. customPurification via flash chromatography (98:2 hexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-ba49046829ca48738843f8ff099ce829
출처 데이터셋
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08524725B2

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