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Nitronium tetrafluoroborate → HCID 21084113、化合物

HRID 2253368
ノート
印刷プレビュー

反応式

HRID 2253368 の反応式
[Br:1][C:2]1[N:7]2[N:8]=[C:9]([CH3:11])[CH:10]=[C:6]2[CH:5]=[CH:4][CH:3]=1.F[B-](F)(F)F.[O:17]=[N+:18]=[O:19]>C(#N)C>[Br:1][C:2]1[N:7]2[N:8]=[C:9]([CH3:11])[C:10]([N+:18]([O-:19])=[O:17])=[C:6]2[CH:5]=[CH:4][CH:3]=1
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 11073463Nitronium tetrafluoroborateHCID 21084115HCID 21084115、化合物

生成物 1

HCID 21084113HCID 21084113、化合物収率 57.1%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

To a solution of 7-bromo-2-methylpyrazolo[1,5-a]pyridine (1.3 g) dissolved in acetonitrile (25 mL) was added nitronium tetrafluoroborate (900 mg) while stirring on ice, and the reaction mixture was stirred for 10 minutes. The obtained reaction mixture was added to ice water, and the precipitated crystals were collected by filtration, washed with water and then dried under reduced pressure to afford crude crystals. These were purified by silica gel column chromatography and the title compound (900 mg) was obtained as yellow crystals from the n-hexane:ethyl acetate (5:1) fraction.

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

後処理

  1. stirringthe reaction mixture was stirred for 10 minutes
  2. customThe obtained reaction mixture
  3. filtrationthe precipitated crystals were collected by filtration
  4. washwashed with water
  5. customdried under reduced pressure
  6. customto afford crude crystals
  7. customThese were purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-ff2c3da4decc4a4294800b36899dd5b7
出典データセット
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07323569B2

反応ノート

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