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1-Bromo-3-chloropropane → 1-(3-Chloropropyl)indolin-2-one

HRID 1751037
ノート
印刷プレビュー

反応式

HRID 1751037 の反応式
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10].Br[CH2:12][CH2:13][CH2:14][Cl:15].C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[Cl:15][CH2:14][CH2:13][CH2:12][N:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][C:2]1=[O:10]
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 3

HCID 80061-Bromo-3-chloropropaneHCID 11430Potassium CarbonateHCID 321710Oxindole

生成物 1

HCID 180699061-(3-Chloropropyl)indolin-2-one

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

Oxindole (2.00 g, 0.0150 mol), 1-bromo-3-chloropropane (2.97 mL, 0.03 mol), and potassium carbonate (4.15 g, 0.03 mol) in acetonitrile (40 mL) were heated at reflux for 20 hours. The mixture was evaporated, diluted with ethyl acetate, washed with 2M aqueous hydrochloric acid and brine, dried (MgSO4), and evaporated. The residue was purified by Biotage flash column chromatography (30% ethyl acetate/hexanes) to give product as an oil which solidified on standing (1.57 g, 50%); MS for C11H12ClNO m/z 210 (M+H)+.

後処理

  1. temperatureat reflux for 20 hours
  2. customThe mixture was evaporated
  3. additiondiluted with ethyl acetate
  4. washwashed with 2M aqueous hydrochloric acid and brine
  5. dry with materialdried (MgSO4)
  6. customevaporated
  7. customThe residue was purified by Biotage flash column chromatography (30% ethyl acetate/hexanes)
  8. customto give product as an oil which

出典と根拠

ORDレコード
ord-6b3a8dd9ca414553ad553e3ccb4c6562
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09156840B2

反応ノート

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