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

HRID 1799571
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HRID 1799571 반응식
[K].[C:2]([O:9][CH2:10][CH3:11])(=[O:8])[C:3]([O:5]CC)=O.[CH3:12][O:13][C:14]1[N:19]=[C:18]([CH3:20])[C:17]([N+:21]([O-:23])=[O:22])=[CH:16][CH:15]=1>C(O)C>[CH3:12][O:13][C:14]1[N:19]=[C:18]([CH2:20][C:3](=[O:5])[C:2]([O:9][CH2:10][CH3:11])=[O:8])[C:17]([N+:21]([O-:23])=[O:22])=[CH:16][CH:15]=1
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참가 물질

5

반응물 3

HCID 7268Diethyl OxalateHCID 2304756-Methoxy-2-methyl-3-nitropyridineHCID 5462222Potassium2회

생성물 1

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

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A roundbottom flask was charged with ethanol (540 ml) and (7.2 L). To this was added potassium (81.6 g, 2.09 mol) and mixture was stirred until all the potassium dissolved. Diethyl oxalate (306 g, 2.10 mol) was then added. The mixture was stirred for 5 minutes and then 6-methoxy-2-methyl-3-nitropyridine (320.0 g, 1.87 mol) was added. The resulting solution was stirred at room temperature for 36 hours. The slurry was filtered and the collected solids were washed thoroughly with ether and dried under reduced pressure. The solid was then suspended in 30 ml of water acetic acid was added until the pH=4. The solids that formed were collected by filtration to afford the title compound.

후처리

  1. dissolutiondissolved
  2. stirringThe resulting solution was stirred at room temperature for 36 hours
  3. filtrationThe slurry was filtered
  4. washthe collected solids were washed thoroughly with ether
  5. customdried under reduced pressure
  6. additionwas added until the pH=4
  7. customThe solids that formed
  8. filtrationwere collected by filtration

출처 및 근거

ORD 기록
ord-7f283420907e42fdabb4b995861cad5b
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08344144B2

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