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

HRID 1841523
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HRID 1841523 반응식
[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]
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참가 물질

4

반응물 2

HCID 459320Ethyl 4-amino-3-iodobenzoateHCID 21225700Diisobutylaluminumhydride

생성물 1

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

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

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온도
0 °C

실험 절차

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, gradient from CH2Cl2 to 2% MeOH/CH2Cl2). Fractions homogeneous by TLC are combined and condensed to afford (4-amino-3-iodophenyl)methanol.

후처리

  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, gradient from CH2Cl2 to 2% MeOH/CH2Cl2)
  10. customcondensed

출처 및 근거

ORD 기록
ord-c6c138aba1374098be5d75bcbcd7f040
출처 데이터셋
uspto-grants-2004_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06683181B2

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