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4-(2-Methoxy-5-nitrophenyl)morpholine → 4-Methoxy-3-morpholin-4-yl-phenylamine

HRID 271107
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인쇄 미리보기

반응식

HRID 271107 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([N+:9]([O-])=O)=[CH:5][C:4]=1[N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1>C(O)C>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH2:9])=[CH:5][C:4]=1[N:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 223531674-(2-Methoxy-5-nitrophenyl)morpholine

생성물 1

HCID 176047884-Methoxy-3-morpholin-4-yl-phenylamine수율 70.4%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

4-(2-Methoxy-5-nitro-phenyl)-morpholine (w, 390 mg) was dissolved in 10 mL ethanol and reduced under 1 atm H2 using 10% Pd—C as a catalyst. After 14 hours, the catalyst was filtered off and the solvent was evaporated, affording 240 mg 4-methoxy-3-morpholin-4-yl-phenylamine (x) which was used without further purification: m/e: 208.12, MS (ES+): 209.2.

후처리

  1. filtrationthe catalyst was filtered off
  2. customthe solvent was evaporated

출처 및 근거

ORD 기록
ord-8c8eee9f0a26434287d5f025231ce4ea
출처 데이터셋
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07452873B2

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