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Diethyl Oxalate → 3-(2-Methyl-5-nitropyridin-4-yl)-2-oxopropionic acid ethyl ester

HRID 1693386
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HRID 1693386 반응식
[O-]CC.[K+].[C:5]([O:12][CH2:13][CH3:14])(=[O:11])[C:6]([O:8]CC)=O.[CH3:15][C:16]1[CH:21]=[C:20]([CH3:22])[C:19]([N+:23]([O-:25])=[O:24])=[CH:18][N:17]=1>C(OCC)C.C(O)C>[CH2:13]([O:12][C:5](=[O:11])[C:6](=[O:8])[CH2:22][C:20]1[C:19]([N+:23]([O-:25])=[O:24])=[CH:18][N:17]=[C:16]([CH3:15])[CH:21]=1)[CH3:14]
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참가 물질

6

반응물 3

HCID 7268Diethyl OxalateHCID 137174802,4-Dimethyl-5-nitropyridineHCID 23670592Potassium ethoxide

생성물 1

HCID 597537363-(2-Methyl-5-nitropyridin-4-yl)-2-oxopropionic acid ethyl ester

시약·촉매·용매 2

HCID 702Ethanol용매2회HCID 3283Diethyl Ether
용매
2회

실험 절차

To a solution of potassium ethoxide (0.262 g, 2.96 mmol) in diethyl ether (10 mL) and ethanol (1 mL) was added diethyl oxalate (0.404 mL, 2.96 mmol) in one portion and the resulting solution stirred for 10 min at rt. 2,4-Dimethyl-5-nitropyridine (Preparation 63, 0.400 g, 2.63 mmol) was added as a suspension in diethyl ether (1 mL)/ethanol (1.5 mL) and stirring continued for 16 h at rt. The mixture was filtered, washing with cold diethyl ether. The collected precipitate was dissolved in water and the pH adjusted to 4 by the addition of glacial acetic acid. The resulting precipitate was collected by filtration and air dried. The solid was partitioned between ethyl acetate (150 mL) and water (50 mL) and the layers separated. The aqueous layer was extracted with ethyl acetate (3×20 mL) and the combined organics washed with brine (50 mL), dried (MgSO4), filtered and concentrated under reduced pressure to give the title compound as a red solid which required no further purification. δH (CDCl3): 1.40 (3H, t), 4.40 (2H, q), 4.52 (2H, s), 7.11 (1H, s), 9.25 (1H, s).

후처리

  1. stirringstirring
  2. waitcontinued for 16 h at rt
  3. filtrationThe mixture was filtered
  4. washwashing with cold diethyl ether
  5. dissolutionThe collected precipitate was dissolved in water
  6. additionthe pH adjusted to 4 by the addition of glacial acetic acid
  7. filtrationThe resulting precipitate was collected by filtration and air
  8. customdried
  9. customThe solid was partitioned between ethyl acetate (150 mL) and water (50 mL)
  10. customthe layers separated
  11. extractionThe aqueous layer was extracted with ethyl acetate (3×20 mL)
  12. washthe combined organics washed with brine (50 mL)
  13. dry with materialdried (MgSO4)
  14. filtrationfiltered
  15. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-9678c844418143e2b8cf15301b2cbab6
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08158622B2

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