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Stannous chloride dihydrate → 2-(3-Aminophenyl)-2-methylpropanenitrile

HRID 631603
ノート
印刷プレビュー

反応式

HRID 631603 の反応式
O.O.[Sn](Cl)Cl.[CH3:6][C:7]([C:11]1[CH:16]=[CH:15][CH:14]=[C:13]([N+:17]([O-])=O)[CH:12]=1)([CH3:10])[C:8]#[N:9]>CCO>[NH2:17][C:13]1[CH:12]=[C:11]([C:7]([CH3:10])([CH3:6])[C:8]#[N:9])[CH:16]=[CH:15][CH:14]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 61436Stannous chloride dihydrateHCID 155413242-Methyl-2-(3-nitrophenyl)propanenitrile

生成物 1

HCID 569657872-(3-Aminophenyl)-2-methylpropanenitrile収率 73%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
90 °C

実験手順

To a suspension of tin (II) chloride bis hydrate (3.3 g, 13.1 mmol) in EtOH (25 mL) was added 2-methyl-2-(3-nitrophenyl)propanenitrile (800 mg, 4.2 mmol). The reaction mixture was stirred at 90° C. for 1 h. After cooling down to rt, the solvent was removed under reduced pressure and the residue taken in DCM, washed with water and a saturated solution of sodium hydrogen carbonate until pH=8. After combining, the organics were dried (MgSO4) and concentrated. The residue was purified by silica gel chromatography (hexane/ethyl acetate 15%) to afford 2-(3-aminophenyl)-2-methylpropanenitrile (490 mg, 73%) as a colorless solid. 1H NMR (300 MHz, CDCl3) δ 1.69 (s, 6H), 3.75 (brs, 2H), 6.64 (d, J=9 Hz, 1H), 6.80-6.83 (m, 2H), 7.15-7.19 (m, 1H); LC-MS (ESI) m/z 161 (M+H)+.

後処理

  1. temperatureAfter cooling down to rt
  2. customthe solvent was removed under reduced pressure
  3. washwashed with water
  4. dry with materialthe organics were dried (MgSO4)
  5. concentrationconcentrated
  6. customThe residue was purified by silica gel chromatography (hexane/ethyl acetate 15%)

出典と根拠

ORDレコード
ord-28d8e61a38e747e582af2f75b23584f6
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09320739B2

反応ノート

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