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Toluene → 1-Methyl-6-nitroindoline

HRID 1939166
ノート
印刷プレビュー

反応式

HRID 1939166 の反応式
C[Si]([N-][Si](C)(C)C)(C)C.[K+].[C:11]1(C)C=CC=CC=1.[N+:18]([C:21]1[CH:29]=[C:28]2[C:24]([CH2:25][CH2:26][NH:27]2)=[CH:23][CH:22]=1)([O-:20])=[O:19].IC>O1CCCC1.CO>[CH3:11][N:27]1[C:28]2[C:24](=[CH:23][CH:22]=[C:21]([N+:18]([O-:20])=[O:19])[CH:29]=2)[CH2:25][CH2:26]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 1140TolueneHCID 6328Methyl iodideHCID 297576-NitroindolineHCID 3251421Potassium bis(trimethylsilyl)amide

生成物 1

HCID 123690471-Methyl-6-nitroindoline

試薬・触媒・溶媒 2

HCID 887Methanol溶媒
HCID 8028
Tetrahydrofuran
溶媒

実験手順

Potassium bis(trimethylsilyl)amide (67 ml of a 0.5M toluene solution) was added slowly to a stirred solution of 6-nitroindoline (5.0 g) in anhydrous tetrahydrofuran (200 ml) at -78° C. under a nitrogen atmosphere. Iodomethane (2.09 ml) was added then the reaction mixture was allowed to warm to room temperature then stirred overnight. Methanol (5 ml) was added then the solution was evaporated to dryness. The residue was dissolved in diethyl ether (300 ml), washed with water, saturated brine then dried (magnesium sulphate) and evaporated to dryness. The crude product was purified by column chromatography on silica using 10% ethyl acetate/petroleum ether (60-80)→30% ethyl acetate/petroleum ether (60-80) and the product crystallised from diethyl ether/petroleum ether (60-80) to afford 0.9 g.

後処理

  1. customthe solution was evaporated to dryness
  2. dissolutionThe residue was dissolved in diethyl ether (300 ml)
  3. washwashed with water, saturated brine
  4. dry with materialthen dried (magnesium sulphate)
  5. customevaporated to dryness
  6. customThe crude product was purified by column chromatography on silica using 10% ethyl acetate/petroleum ether (60-80)→30% ethyl acetate/petroleum ether (60-80)
  7. customthe product crystallised from diethyl ether/petroleum ether (60-80)
  8. customto afford 0.9 g

出典と根拠

ORDレコード
ord-7050f3be52e54fcc98c5f41695d63839
出典データセット
uspto-grants-1997_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05696110

反応ノート

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