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Sodium ethoxide → HCID 89826007, 화합물

HRID 1775373
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HRID 1775373 반응식
[Br:1][C:2]1[CH:7]=[C:6]([N+]([O-])=O)[CH:5]=[C:4]([CH3:11])[N+:3]=1[O-:12].[O-:13][CH2:14][CH3:15].[Na+]>C(O)C>[Br:1][C:2]1[CH:7]=[C:6]([O:13][CH2:14][CH3:15])[CH:5]=[C:4]([CH3:11])[N+:3]=1[O-:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 2723922Sodium ethoxideHCID 27518162-Bromo-6-methyl-4-nitro-1-oxo-1lambda~5~-pyridine

생성물 1

HCID 89826007HCID 89826007, 화합물수율 84%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

2-Bromo-6-methyl-4-nitro-pyridine 1-oxide (1 g, 4.3 mmol) was dissolved in ethanol (anhydrous, 50 ml), and sodium ethoxide (21% in ethanol, 1.4 ml, 4.3 mmol) was added dropwise with stirring. The mixture was stirred at room temperature overnight, concentrated under reduced pressure, the residue was taken up in DCM (50 ml), the mixture was washed with water (50 ml), dried (sodium sulfate) and concentrated under reduced pressure to yield 0.84 g of brown yellow crystals (3.6 mmol, 84%).

후처리

  1. stirringThe mixture was stirred at room temperature overnight
  2. concentrationconcentrated under reduced pressure
  3. washthe mixture was washed with water (50 ml)
  4. dry with materialdried (sodium sulfate)
  5. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-e5ae67b001544e7cbbf79b18a5c49923
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09260441B2

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