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Potassium Carbonate → HCID 58476611, 화합물

HRID 1892210
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HRID 1892210 반응식
[CH3:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:5]([C:11]#[C:12][Si](C)(C)C)=[CH:4][N:3]=1.C(=O)([O-])[O-].[K+].[K+]>CO>[C:11]([C:5]1[CH:6]=[C:7]([N+:8]([O-:10])=[O:9])[C:2]([CH3:1])=[N:3][CH:4]=1)#[CH:12]
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참가 물질

4

반응물 2

HCID 11430Potassium CarbonateHCID 59404985HCID 59404985, 화합물

생성물 1

HCID 58476611HCID 58476611, 화합물수율 92.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 2-methyl-3-nitro-5-[(trimethylsilyl)ethynyl]pyridine (2.32 g, 9.90 mmol) in methanol (22 mL) was cooled to 0° C. and potassium carbonate (137 mg, 0.99 mmol) was added. The reaction mixture was allowed to warm and stir at rt for 10 min, during which time a yellow precipitate formed. The reaction mixture was then concentrated and diluted with ether (200 mL). The organic solution was washed with water (200 mL) and brine (200 mL), dried over MgSO4, filtered and concentrated to give 5-ethynyl-2-methyl-3-nitropyridine (1.48 g, 92%) as a solid. LCMS (FA): Rt=1.64 min, m/z=163.0 (M+H).

후처리

  1. temperatureto warm
  2. customformed
  3. concentrationThe reaction mixture was then concentrated
  4. additiondiluted with ether (200 mL)
  5. washThe organic solution was washed with water (200 mL) and brine (200 mL)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-079396021b2742f182c23a928f843711
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507667B2

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