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Tert-Butyl nitrite → 2,5-Dimethyl-1,3-dinitrobenzene

HRID 618259
ノート
印刷プレビュー

反応式

HRID 618259 の反応式
N(OC(C)(C)C)=O.[CH3:8][C:9]1[C:10]([N+:20]([O-:22])=[O:21])=[C:11](N)[C:12]([CH3:18])=[CH:13][C:14]=1[N+:15]([O-:17])=[O:16]>CN(C)C=O>[CH3:8][C:9]1[C:10]([N+:20]([O-:22])=[O:21])=[CH:11][C:12]([CH3:18])=[CH:13][C:14]=1[N+:15]([O-:17])=[O:16]
参加物反応条件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 10906Tert-Butyl nitriteHCID 2387023,6-Dimethyl-2,4-dinitroaniline

生成物 1

HCID 124560182,5-Dimethyl-1,3-dinitrobenzene収率 83.4%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

反応条件

温度
65 °C

実験手順

To a solution of t-butyl nitrite (t-BuONO) (7.32 g) in dimethyl formamide (DMF) (50 mL, from Mallinckrodt) at 65° C. was added dropwise a solution of 3,6-dimethyl-2.4-dinitro-phenylamine (10 g, from above) in DMF (50 mL) during 5-10 min. The mixture was heated at 65° C. for 15 min and the solvent was removed under reduced pressure. The residue was partitioned between dichloromethane (300 mL) and half-saturated sodium chloride solution. The dichloromethane solution was washed with additional half-saturated sodium chloride solution (300 mL) and dried over magnesium sulfate. After evaporation of the solvent, the residue was taken up in dichloromethane (250 mL) and passed through a short column (silica gel). Eluting with dichloromethane gave 2,5-dimethyl-1,3-dinitro-benzene (7.75 g).

後処理

  1. customthe solvent was removed under reduced pressure
  2. customThe residue was partitioned between dichloromethane (300 mL) and half-saturated sodium chloride solution
  3. washThe dichloromethane solution was washed with additional half-saturated sodium chloride solution (300 mL)
  4. dry with materialdried over magnesium sulfate
  5. customAfter evaporation of the solvent
  6. washEluting with dichloromethane

出典と根拠

ORDレコード
ord-0950ac8515104a028690422a972acae9
出典データセット
uspto-grants-1999_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05952362

反応ノート

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