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2-Morpholin-4-yl-5-nitrophenol → 5-Amino-2-morpholinophenol

HRID 929687
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반응식

HRID 929687 반응식
[O:1]1[CH2:6][CH2:5][N:4]([C:7]2[CH:12]=[CH:11][C:10]([N+:13]([O-])=O)=[CH:9][C:8]=2[OH:16])[CH2:3][CH2:2]1>[Pd].C(O)C.[H][H]>[NH2:13][C:10]1[CH:11]=[CH:12][C:7]([N:4]2[CH2:3][CH2:2][O:1][CH2:6][CH2:5]2)=[C:8]([OH:16])[CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 230715652-Morpholin-4-yl-5-nitrophenol

생성물 1

HCID 539059685-Amino-2-morpholinophenol수율 105%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 702Ethanol용매HCID 178418361HCID 178418361, 화합물용매

실험 절차

10% Palladium on carbon (10 mg, 0.892 mmol) was added to 2-morpholino-5-nitrophenol (prepared as described herein above; 200 mg, 0.892 mmol) in ethanol (20 mL), hydrogen gas was added (40 psi), and the reaction allowed to proceed for 12 h at room temperature. The reaction was monitored by TLC. After completion of the reaction, the reaction mixture filtered through Celite®, and the solvent removed in vacuo. The residue was purified by flash column chromatography (2% CH3OH/CH2Cl2) to provide the title compound 5-amino-2-morpholinophenol (200 mg, 0.937 mmol, 105% yield) as a solid.

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후처리

  1. additionwas added (40 psi)
  2. customAfter completion of the reaction
  3. filtrationthe reaction mixture filtered through Celite®
  4. customthe solvent removed in vacuo
  5. customThe residue was purified by flash column chromatography (2% CH3OH/CH2Cl2)

출처 및 근거

ORD 기록
ord-c08b78cf3cda4d8abdf7fbec3f3950df
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09296703B2

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