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

HRID 1264988
ノート
印刷プレビュー

反応式

HRID 1264988 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-673c0a129c7445948634d4a491515384
出典データセット
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06544990B2

反応ノート

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