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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4'-Fluoro-2'-methoxy-4-nitrobiphenyl → 4'-Fluoro-2'-methoxy[1,1'-biphenyl]-4-amine

HRID 442267
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인쇄 미리보기

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HRID 442267 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([N+:14]([O-])=O)=[CH:10][CH:9]=2)=[C:4]([O:17][CH3:18])[CH:3]=1.[H][H]>[Pd].C(O)C>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([NH2:14])=[CH:10][CH:9]=2)=[C:4]([O:17][CH3:18])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 214164654'-Fluoro-2'-methoxy-4-nitrobiphenylHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 214164544'-Fluoro-2'-methoxy[1,1'-biphenyl]-4-amine

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

A mixture of 10 grams of 4'-fluoro-2'-methoxy-4-nitrobiphenyl in 250 ml. of ethanol is reduced by hydrogen at atmospheric pressure and at room temperature using 5% palladium-on-charcoal (0.5 gram) catalyst. After the required uptake of hydrogen, the mixture is filtered and the catalyst washed with fresh ethanol. The ethanol solution is then concentrated in vacuo, and the residue recrystallized from aqueous ethanol to yield 4-(4'-fluoro-2'-methoxyphenyl)-aniline.

후처리

  1. filtrationAfter the required uptake of hydrogen, the mixture is filtered
  2. washthe catalyst washed with fresh ethanol
  3. concentrationThe ethanol solution is then concentrated in vacuo
  4. customthe residue recrystallized from aqueous ethanol

출처 및 근거

ORD 기록
ord-b68a5fb89a654044a40c3a10d2f81774
출처 데이터셋
uspto-grants-1977_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04044049

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