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Diethyl Oxalate → Ethyl 3-(6-methoxy-3-nitropyridin-2-yl)-2-oxopropanoate

HRID 751628
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HRID 751628 반응식
[O-]CC.[K+].[C:5]([O:12][CH2:13][CH3:14])(=[O:11])[C:6]([O:8]CC)=O.[CH3:15][O:16][C:17]1[N:22]=[C:21]([CH3:23])[C:20]([N+:24]([O-:26])=[O:25])=[CH:19][CH:18]=1>C(OCC)C.C(O)C>[CH2:13]([O:12][C:5](=[O:11])[C:6](=[O:8])[CH2:23][C:21]1[C:20]([N+:24]([O-:26])=[O:25])=[CH:19][CH:18]=[C:17]([O:16][CH3:15])[N:22]=1)[CH3:14]
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참가 물질

6

반응물 3

HCID 7268Diethyl OxalateHCID 2304756-Methoxy-2-methyl-3-nitropyridineHCID 23670592Potassium ethoxide

생성물 1

HCID 59753655Ethyl 3-(6-methoxy-3-nitropyridin-2-yl)-2-oxopropanoate

시약·촉매·용매 2

HCID 702Ethanol용매HCID 3283Diethyl Ether용매2회

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온도
0 °C

실험 절차

To a stirred suspension of potassium ethoxide (0.55 g, 6.55 mmol) in diethyl ether (20 mL, anhydrous) and ethanol (4 mL) was added diethyl oxalate (894 μL, 6.55 mmol) and the reaction mixture was stirred for 30 min prior to the addition of 6-methoxy-2-methyl-3-nitropyridine (Preparation 33, 1.0 g, 5.95 mmol) in diethyl ether (8 mL). The resulting red suspension was stirred at rt, under argon, for 20 h. The mixture was filtered, the solid washed thoroughly with diethyl ether then dried. The red solid was then taken up in hot water and the solution cooled to 0° C. The precipitate was filtered, washed with cold water, and dried to give the title compound as a beige solid. δH (CDCl3): 1.40 (3H, t), 4.07 (3H, s), 4.39 (2H, q), 6.74 (1H, d), 7.57 (1H, s), 8.40 (1H, d), 13.82 (1H, s).

후처리

  1. stirringThe resulting red suspension was stirred at rt, under argon, for 20 h
  2. filtrationThe mixture was filtered
  3. washthe solid washed thoroughly with diethyl ether
  4. customthen dried
  5. filtrationThe precipitate was filtered
  6. washwashed with cold water
  7. customdried

출처 및 근거

ORD 기록
ord-a4de3c39692d49fe8c4ff464c7f6d4d7
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07405210B2

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