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Water → 3-Iodo-4-(2-methoxyethoxy)aniline

HRID 1593766
ノート
印刷プレビュー

反応式

HRID 1593766 の反応式
[Cl-].[NH4+].O.[I:4][C:5]1[CH:10]=[C:9]([N+:11]([O-])=O)[CH:8]=[CH:7][C:6]=1[O:14][CH2:15][CH2:16][O:17][CH3:18]>C(O)C.[Fe]>[I:4][C:5]1[CH:10]=[C:9]([NH2:11])[CH:8]=[CH:7][C:6]=1[O:14][CH2:15][CH2:16][O:17][CH3:18]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 962WaterHCID 25517Ammonium ChlorideHCID 69310862HCID 69310862、化合物

生成物 1

HCID 660942063-Iodo-4-(2-methoxyethoxy)aniline収率 58.8%

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 702Ethanol溶媒

実験手順

A suspension of iron (3.89 g, 69.7 mmol), ammonium chloride (5.0 g, 93.5 mmol), in 100 mL of ethanol and 28 mL of water was heated to reflux. 2-Iodo-1-(2-methoxyethoxy)-4-nitrobenzene (7.5 g, 23.2 mmol) was added and the reaction was heated at reflux for 3 hours. The mixture was cooled to room temperature and filtered through Celite, washed with ethanol. The filtrate was concentrated in vacuo until a precipitate appeared. The precipitate was removed by filtration through Magnesol and the filtrate was concentrated in vacuo to provide 4.0 g of [3-iodo-4-(2-methoxyethoxy)phenyl]amine as an oil; 1H NMR (300 MHz, DMSO-d6) δ 3.33 (s, 3H), 3.62 (t, 2H), 3.95 (t, 2H), 5.01 (d, 2H), 6.55 (d, 1H), 6.73 (d, 1H), 7.03 (s, 1H); MS (ES) m/z294.0 (M+H)

後処理

  1. temperaturethe reaction was heated
  2. temperatureat reflux for 3 hours
  3. filtrationfiltered through Celite
  4. washwashed with ethanol
  5. concentrationThe filtrate was concentrated in vacuo until a precipitate
  6. customThe precipitate was removed by filtration through Magnesol
  7. concentrationthe filtrate was concentrated in vacuo

出典と根拠

ORDレコード
ord-b1267d0101b0479ba5b1f6cb26cf075d
出典データセット
uspto-grants-2007_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07297795B2

反応ノート

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