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Methyl iodide → 2-chloro-N-methyl-5-nitroaniline

HRID 1591611
ノート
印刷プレビュー

反応式

HRID 1591611 の反応式
[H-].[Na+].[Cl:3][C:4]1[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:5]=1[NH2:6].I[CH3:15]>O1CCCC1>[Cl:3][C:4]1[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:5]=1[NH:6][CH3:15]
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 6328Methyl iodideHCID 226912-Chloro-5-nitroanilineHCID 24758Sodium hydride

生成物 1

HCID 37209232-chloro-N-methyl-5-nitroaniline収率 33.3%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒3 回

実験手順

To a suspension of sodium hydride (60% in oil, 1.2 g, 30 mmol) in tetrahydrofuran (100 ml), cooled in an ice bath, was added slowly a solution of 2-chloro-5-nitroaniline (5 g, 29 mmol) in tetrahydrofuran (10 ml) followed by a solution of iodomethane (1.8 ml, 29 mmol) in tetrahydrofuran (10 ml). After stirring at room temperature for 20 hours, the mixture was concentrated under reduced pressure and the residue was partitioned between dichloromethane (100 ml) and water (100 ml). The organic layer was washed with saturated aqueous sodium chloride solution (50 ml), dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with dichloromethane-hexane (1:3) and recrystalized (ethyl ether) to provide (2-chloro-5-nitro-phenyl)-methyl-amine (1.8 g, 33% yield) as orange crystals.

後処理

  1. temperaturecooled in an ice bath
  2. concentrationthe mixture was concentrated under reduced pressure
  3. customthe residue was partitioned between dichloromethane (100 ml) and water (100 ml)
  4. washThe organic layer was washed with saturated aqueous sodium chloride solution (50 ml)
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by flash chromatography on silica gel eluting with dichloromethane-hexane (1:3)
  8. customrecrystalized (ethyl ether)

出典と根拠

ORDレコード
ord-3b803f6ae44e474094360ae8fabd766c
出典データセット
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07291616B2

反応ノート

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