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4-Nitro-1,3-dihydro-2H-indol-2-one → 4-Aminoindolin-2-one

HRID 1275664
ノート
印刷プレビュー

反応式

HRID 1275664 の反応式
[N+:1]([C:4]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:5]=1[CH2:6][C:7](=[O:13])[NH:8]2)([O-])=O>CO.[Pd]>[NH2:1][C:4]1[CH:12]=[CH:11][CH:10]=[C:9]2[C:5]=1[CH2:6][C:7](=[O:13])[NH:8]2
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 1

HCID 216778744-Nitro-1,3-dihydro-2H-indol-2-one

生成物 1

HCID 122374724-Aminoindolin-2-one収率 76%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

A catalytic amount of 10% palladium-on-carbon is added to a solution of 4-nitrooxindole (0.889 g, 4.99 mmol) in methanol (100 mL). The suspension is degassed three times and placed under an atmosphere of hydrogen for 3 hours. The suspension is filtered through a pad of Celite and the Celite is washed several times with methanol. The methanol from the filtrate is removed by rotary evaporation. The resulting residue is purified via silica gel column chromatography using 3% methanol/methylene chloride as the eluent. The appropriate fractions are combined and the solvents removed by rotary evaporation to yield 0.558 g of 4-aminooxindole as a light orange solid (76%).

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. customThe suspension is degassed three times
  2. filtrationThe suspension is filtered through a pad of Celite
  3. washthe Celite is washed several times with methanol
  4. customThe methanol from the filtrate is removed by rotary evaporation
  5. customThe resulting residue is purified via silica gel column chromatography
  6. customthe solvents removed by rotary evaporation

出典と根拠

ORDレコード
ord-8f12cb5d5bc64dd8a0f17997aeb65b51
出典データセット
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06162818

反応ノート

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