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Ethyl 4-amino-3-iodobenzoate → (4-Amino-3-iodophenyl)methanol

HRID 2086604
ノート
印刷プレビュー

反応式

HRID 2086604 の反応式
[NH2:1][C:2]1[CH:12]=[CH:11][C:5]([C:6](OCC)=[O:7])=[CH:4][C:3]=1[I:13].[H-].C([Al+]CC(C)C)C(C)C>C(Cl)Cl>[NH2:1][C:2]1[CH:12]=[CH:11][C:5]([CH2:6][OH:7])=[CH:4][C:3]=1[I:13]
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 459320Ethyl 4-amino-3-iodobenzoateHCID 21225700Diisobutylaluminumhydride

生成物 1

HCID 22724559(4-Amino-3-iodophenyl)methanol

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

反応条件

温度
0 °C

実験手順

To a solution of ethyl 4-amino-3-iodobenzoate (8.0 g) in CH2Cl2 (56 mL) cooled to 0° C. is added diisobutylaluminum hydride in CH2Cl2 (110 mL of a 1M solution). The reaction is stirred at 0° C. for 2 h then quenched by the addition of MeOH (50 mL). To this is added 1N HCl (100 mL). The mixture is concentrated to remove the organics. The aqueous solution is extracted with CH2Cl2 (3×). The combined organic layers are dried over Na2SO4, filtered and condensed. The resulting residue is adsorbed onto silica and chromatographed (Biotage flash 40M, eluent CH2Cl2 (2L), 1% MeOH/CH2Cl2 (2L), 2% MeOH/CH2Cl2). Fractions homogeneous by TLC are combined and condensed to afford (4-amino-3-iodophenyl)methanol.

後処理

  1. customthen quenched by the addition of MeOH (50 mL)
  2. additionTo this is added 1N HCl (100 mL)
  3. concentrationThe mixture is concentrated
  4. customto remove the organics
  5. extractionThe aqueous solution is extracted with CH2Cl2 (3×)
  6. dry with materialThe combined organic layers are dried over Na2SO4
  7. filtrationfiltered
  8. customcondensed
  9. customchromatographed (Biotage flash 40M, eluent CH2Cl2 (2L), 1% MeOH/CH2Cl2 (2L), 2% MeOH/CH2Cl2)
  10. customcondensed

出典と根拠

ORDレコード
ord-57402e57040a44be9a47e449cd982f7e
出典データセット
uspto-grants-2004_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06727248B2

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