3,5-Dimethoxyaniline → 3-Amino-5-methoxyphenol

HRID 881976ノート

反応式

HRID 881976 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:7]=[C:8]([O:10]C)[CH:9]=1)[NH2:6].C[S-].[Na+]>CN1CCCC1=O>[NH2:6][C:5]1[CH:7]=[C:8]([OH:10])[CH:9]=[C:3]([O:2][CH3:1])[CH:4]=1

参加物

4

反応条件

温度
140 °C

実験手順

To a solution of 3,5-dimethoxyaniline (2.53 g, 16.5 mmol) in N-methylpyrrolidinone (10 ml) was added sodium thiomethoxide (2.32 g, 33.1 mmol). The reaction mixture was heated to 140° C. for 2.5 hours and then stirred at ambient temperature for a further 18 hours. The mixture was poured into a saturated solution of NaH2PO4 (50 ml) and then extracted with ethyl acetate. The combined organic layers were filtered through a hydrophobic frit and the solvent was removed under reduced pressure to give a dark red oil. The crude residue was purified by normal phase chromatography, eluting with iso-hexane and increasing amounts of ethyl acetate to give 3-amino-5-methoxyphenol, as a pale yellow solid (1.53 g).

後処理

  1. extractionextracted with ethyl acetate
  2. filtrationThe combined organic layers were filtered through a hydrophobic frit
  3. customthe solvent was removed under reduced pressure
  4. customto give a dark red oil
  5. customThe crude residue was purified by normal phase chromatography
  6. washeluting with iso-hexane
  7. temperatureincreasing amounts of ethyl acetate

出典と根拠

ORDレコード
ord-fdf8b9c77abb4fea93fd3dedac32d7f2
出典データセット
uspto-grants-2015_03
特許番号
US08993757B2

反応ノート

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