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Potassium Carbonate → HCID 58476611、化合物

HRID 2388011
ノート
印刷プレビュー

反応式

HRID 2388011 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 11430Potassium CarbonateHCID 59404985HCID 59404985、化合物

生成物 1

HCID 58476611HCID 58476611、化合物収率 92.2%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-92d8e47b938d4b0889d286f3e868e977
出典データセット
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08268992B2

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート