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Nitric Acid → 6-Nitro-2H-pyrido[3,2-B][1,4]oxazin-3(4H)-one

HRID 226901
ノート
印刷プレビュー

反応式

HRID 226901 の反応式
[O:1]1[CH2:6][C:5](=[O:7])[NH:4][C:3]2[N:8]=[CH:9][CH:10]=[CH:11][C:2]1=2.[N+:12]([O-])([OH:14])=[O:13]>C(O)(=O)C.C(OC(=O)C)(=O)C>[N+:12]([C:9]1[CH:10]=[CH:11][C:2]2[O:1][CH2:6][C:5](=[O:7])[NH:4][C:3]=2[N:8]=1)([O-:14])=[O:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 944Nitric AcidHCID 884992H-pyrido(3,2-b)-1,4-oxazin-3(4H)-one

生成物 1

HCID 220607326-Nitro-2H-pyrido[3,2-B][1,4]oxazin-3(4H)-one

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒HCID 7918Acetic Anhydride溶媒

実験手順

2H-Pyrido[3,2-b]-1,4-oxazin-3(4H)-one (2.5 g) was dissolved in acetic acid (6 mL) and acetic anhydride (30 mL). Fuming nitric acid (3 mL) was added dropwise to the reaction solution in ice-bath. The reaction solution was stirred in ice-bath overnight. Solution was poured into crashed ice. The light yellow precipitation was collected by filtration, washed with water and dried to give a mixture of nitrated products (regio-isomers). The mixture was crystallized from dichloromethane to give 6-nitro-2H-pyrido[3,2-b]-1,4-oxazin-3(4H)-one (1 g) as a light yellow solid.

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. additionSolution was poured
  2. customThe light yellow precipitation
  3. filtrationwas collected by filtration
  4. washwashed with water
  5. customdried
  6. customto give
  7. additiona mixture of nitrated products (regio-isomers)
  8. customThe mixture was crystallized from dichloromethane

出典と根拠

ORDレコード
ord-2117e86a9c3c4130b6c0cf5fca8ff167
出典データセット
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07557210B2

反応ノート

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