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3,3-Dibromo-2-oxo-2,3-dihydro-1H-indole-5-carbonitrile → 2-Oxo-2,3-dihydro-1H-indole-5-carbonitrile

HRID 843995
ノート
印刷プレビュー

反応式

HRID 843995 の反応式
Br[C:2]1(Br)[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:11]#[N:12])[CH:9]=2)[NH:4][C:3]1=[O:13]>C(O)(=O)C.[Zn]>[O:13]=[C:3]1[CH2:2][C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:11]#[N:12])[CH:9]=2)[NH:4]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 1

HCID 138640893,3-Dibromo-2-oxo-2,3-dihydro-1H-indole-5-carbonitrile

生成物 1

HCID 27733462-Oxo-2,3-dihydro-1H-indole-5-carbonitrile収率 36.1%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 176Acetic Acid溶媒

実験手順

A solution of 3,3-Dibromo-2-oxo-2,3-dihydro-1H-indole-5-carbonitrile (10.5 grams, 33.3 mmole) and Zn dust (22.0 grams, 338.5 mmole) in acetic acid (250 ml) was stirred at room temperature for 45 minutes. The mixture was filtered through celite and concentrated to dryness. The resulting oil was diluted with 300 ml water and extracted with ethyl acetate. The combined extracts were washed with 1 N sodium hydroxide and brine, dried over MgSO4, filtered, and concentrated to give a white solid (1.9 g). MW 158.

後処理

  1. filtrationThe mixture was filtered through celite and
  2. concentrationconcentrated to dryness
  3. additionThe resulting oil was diluted with 300 ml water
  4. extractionextracted with ethyl acetate
  5. washThe combined extracts were washed with 1 N sodium hydroxide and brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-363855d9d1804ac4b5dcda75788b2561
出典データセット
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06380218B1

反応ノート

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