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4-Nitrophenyl 4-nitrobenzoate → 4-Aminophenyl 4-aminobenzoate

HRID 1158595
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인쇄 미리보기

반응식

HRID 1158595 반응식
[N+:1]([C:4]1[CH:21]=[CH:20][C:7]([C:8]([O:10][C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-])=O)=[CH:13][CH:12]=2)=[O:9])=[CH:6][CH:5]=1)([O-])=O.[H][H]>C(OCC)(=O)C.[Pd]>[NH2:1][C:4]1[CH:21]=[CH:20][C:7]([C:8]([O:10][C:11]2[CH:16]=[CH:15][C:14]([NH2:17])=[CH:13][CH:12]=2)=[O:9])=[CH:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 3470614-Nitrophenyl 4-nitrobenzoateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 154917254-Aminophenyl 4-aminobenzoate수율 100%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8857Ethyl Acetate용매

실험 절차

11.0 g of 4-nitrophenyl 4-nitrobenzoate (38.2 mM) were dissolved in 350 ml of ethyl acetate and 1.0 g of palladium on charcoal (10%) was added. The resulting mixture was hydrogenated at atmospheric pressure until the theoretical amount of hydrogen was consumed. The mixture was then filtered, the cake was washed with ethyl acetate and the filtrate was evaporated to dryness to give 8.71 g (38.2 mM, 99%) of 4-aminophenyl 4-aminobenzoate as slightly beige crystals.

후처리

  1. customwas consumed
  2. filtrationThe mixture was then filtered
  3. washthe cake was washed with ethyl acetate
  4. customthe filtrate was evaporated to dryness

출처 및 근거

ORD 기록
ord-0a9e4faf398c484196c9cf45cfefb593
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07811642B2

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