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Methyl 3'-nitro[1,1'-biphenyl]-4-carboxylate → Methyl 4-(3-aminophenyl)benzoate

HRID 1449507
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인쇄 미리보기

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HRID 1449507 반응식
[N+:1]([C:4]1[CH:5]=[C:6]([C:10]2[CH:15]=[CH:14][C:13]([C:16]([O:18][CH3:19])=[O:17])=[CH:12][CH:11]=2)[CH:7]=[CH:8][CH:9]=1)([O-])=O>O1CCCC1.[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]([C:10]2[CH:15]=[CH:14][C:13]([C:16]([O:18][CH3:19])=[O:17])=[CH:12][CH:11]=2)[CH:7]=[CH:8][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 2753361Methyl 3'-nitro[1,1'-biphenyl]-4-carboxylate

생성물 1

HCID 1393986Methyl 4-(3-aminophenyl)benzoate수율 98.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 8028Tetrahydrofuran용매

실험 절차

In 100 ml of tetrahydrofuran was dissolved 2.70 g of methyl 3'-nitro-biphenyl-4-carboxylate obtained in Reference Example 8. To the solution was added 1.0 g of 10% palladium-on-carbon and the mixture was subjected to catalytic reduction for 2 hours. After removing the catalyst by filtration, the solvent was removed under reduced pressure to obtain 2.34 g of the titled compound.

후처리

  1. customobtained in Reference Example 8
  2. customAfter removing the catalyst
  3. filtrationby filtration
  4. customthe solvent was removed under reduced pressure

출처 및 근거

ORD 기록
ord-da207b51dff04d0497f68fd1ffe0089e
출처 데이터셋
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05599813

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