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Stannous chloride dihydrate → 4-Methoxy-3-[2-(morpholin-4-yl)ethoxy]aniline

HRID 2174480
ノート
印刷プレビュー

反応式

HRID 2174480 の反応式
[CH3:1][O:2][C:3]1[CH:17]=[CH:16][C:15]([N+:18]([O-])=O)=[CH:14][C:4]=1[O:5][CH2:6][CH2:7][N:8]1[CH2:13][CH2:12][O:11][CH2:10][CH2:9]1.O.O.[Sn](Cl)Cl>CCO>[CH3:1][O:2][C:3]1[CH:17]=[CH:16][C:15]([NH2:18])=[CH:14][C:4]=1[O:5][CH2:6][CH2:7][N:8]1[CH2:13][CH2:12][O:11][CH2:10][CH2:9]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 22496148HCID 22496148、化合物

生成物 1

HCID 186726704-Methoxy-3-[2-(morpholin-4-yl)ethoxy]aniline収率 47.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
60 °C

実験手順

4-(2-(2-methoxy-5-nitrophenoxy)ethyl)morpholine (350 mg, 1.2 mmol, 1 eq.) and tin (II) chloride dihydrate (1.4 g, 6.20 mmol, 5 eq.) were placed in EtOH (12.3 mL). The reaction mixture was heated at 60° C. and stirred for 19 hours. The reaction mixture was then concentrated under reduced pressure and the resulting residue was diluted with ethyl acetate. The organic phase was washed with a 1N NaOH aqueous solution, dried over MgSO4, filtered and concentrated under reduced pressure. The resulting residue was purified by column chromatography on silica gel to afford 4-methoxy-3-(2-morpholinoethoxy)aniline (143 mg, 46%).

後処理

  1. concentrationThe reaction mixture was then concentrated under reduced pressure
  2. additionthe resulting residue was diluted with ethyl acetate
  3. washThe organic phase was washed with a 1N NaOH aqueous solution
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe resulting residue was purified by column chromatography on silica gel

出典と根拠

ORDレコード
ord-7889e8994b76452eb68ab2fd6174dde1
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09061999B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート