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2-(4-Nitrophenyl)-1,3-dioxolane → 4-(1,3-Dioxolan-2-yl)aniline

HRID 1039833
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인쇄 미리보기

반응식

HRID 1039833 반응식
C(=O)(O)[O-].[Na+].[N+:6]([C:9]1[CH:14]=[CH:13][C:12]([CH:15]2[O:19][CH2:18][CH2:17][O:16]2)=[CH:11][CH:10]=1)([O-])=O>CCO.[Pt](=O)=O>[O:16]1[CH2:17][CH2:18][O:19][CH:15]1[C:12]1[CH:13]=[CH:14][C:9]([NH2:6])=[CH:10][CH:11]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 2667962-(4-Nitrophenyl)-1,3-dioxolaneHCID 516892Sodium Bicarbonate

생성물 1

HCID 111266244-(1,3-Dioxolan-2-yl)aniline수율 96.9%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매

실험 절차

To a mixture of platinum dioxide (227 mg, 1.00 mmol) and sodium bicarbonate (420 mg, 5.00 mmol) under dry nitrogen was added a solution of 2-(4-nitrophenyl)-1,3-dioxolane (976 mg, 5.00 mmol) in EtOH (30.0 mL). The reaction mixture was bubbled with hydrogen for 15 min and then stirred under a hydrogen atmosphere (balloon) for 2 h. The reaction mixture was then filtered through a pad of Celite washing with MeOH. The filtrate was concentrated under reduced pressure to give the title compound (0.80 g, 96% yield).

후처리

  1. customThe reaction mixture was bubbled with hydrogen for 15 min
  2. filtrationThe reaction mixture was then filtered through a pad of Celite
  3. washwashing with MeOH
  4. concentrationThe filtrate was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-b866c449b7544f51991c8034e5d35fef
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08551978B2

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