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1-[4-(4-Nitrophenoxy)phenyl]ethanone → 1-[4-(4-Aminophenoxy)phenyl]ethan-1-one

HRID 1474639
노트
인쇄 미리보기

반응식

HRID 1474639 반응식
[N+:1]([C:4]1[CH:19]=[CH:18][C:7]([O:8][C:9]2[CH:14]=[CH:13][C:12]([C:15](=[O:17])[CH3:16])=[CH:11][CH:10]=2)=[CH:6][CH:5]=1)([O-])=O>CO.[Pd]>[NH2:1][C:4]1[CH:5]=[CH:6][C:7]([O:8][C:9]2[CH:14]=[CH:13][C:12]([C:15](=[O:17])[CH3:16])=[CH:11][CH:10]=2)=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 2386041-[4-(4-Nitrophenoxy)phenyl]ethanone

생성물 1

HCID 7892361-[4-(4-Aminophenoxy)phenyl]ethan-1-one수율 99.3%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매2회

실험 절차

To a solution of 1-(4-(4-nitrophenoxy)phenyl)ethanone (9.0 g, 35.02 mmol), in methanol (50 mL) under nitrogen atmosphere, was added a solution of 10% palladium on charcoal (1.80 g, 20% by weight) in methanol (20 mL). The reaction mixture was evacuated and purged with hydrogen balloon and stirred at r.t for 6 h. After the completion of reaction as confirmed by TLC, the reaction mixture was brought under nitrogen atmosphere. The reaction mixture was filtered through celite. The filtrate was concentrated in vacuo to afford the title compound (7.90 g, 99%) as a solid.

후처리

  1. customThe reaction mixture was evacuated
  2. custompurged with hydrogen balloon
  3. customAfter the completion of reaction
  4. filtrationThe reaction mixture was filtered through celite
  5. concentrationThe filtrate was concentrated in vacuo

출처 및 근거

ORD 기록
ord-202f8a20930d4b88982a5df8828d8aa5
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09018249B2

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