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4-(3-Nitrophenyl)morpholine → 3-(Morpholin-4-yl)aniline

HRID 31401
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인쇄 미리보기

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HRID 31401 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([N:10]2[CH2:15][CH2:14][O:13][CH2:12][CH2:11]2)[CH:7]=[CH:8][CH:9]=1)([O-])=O.[H][H]>[Pd].C(O)C.CN(C)C=O>[N:10]1([C:6]2[CH:5]=[C:4]([NH2:1])[CH:9]=[CH:8][CH:7]=2)[CH2:11][CH2:12][O:13][CH2:14][CH2:15]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 12532734-(3-Nitrophenyl)morpholine2회HCID 178418361HCID 178418361, 화합물

생성물 1

HCID 8477683-(Morpholin-4-yl)aniline수율 75.3%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 702Ethanol용매HCID 6228Dimethylformamide용매

실험 절차

A flask containing 5% palladium on carbon (1.95 g) was evacuated and refilled with hydrogen. 4-(3-Nitrophenyl)morpholine (intermediate 2) (19.5 g, 93.75 mmol) was introduced into the flask as a solution in ethanol and dimethylformamide (1000 ml, 4:1 v/v). The reaction was stirred at room temperature until further uptake of hydrogen ceased (after approximately 7 L). The reaction was then filtered through celite and solvent removed in vacuo to yield the desired product (12.6 g, 70.6 mmol) as a beige solid.

후처리

  1. customwas evacuated
  2. additionrefilled with hydrogen
  3. filtrationThe reaction was then filtered through celite and solvent
  4. customremoved in vacuo

출처 및 근거

ORD 기록
ord-a15244507528437e925a9edd6315cfe9
출처 데이터셋
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07425555B2

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