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2-fluoro-N,N-di-n-hexyl-4-nitroaniline → HCID 117966053, 화합물

HRID 56147
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HRID 56147 반응식
[F:1][C:2]1[CH:20]=[C:19]([N+:21]([O-])=O)[CH:18]=[CH:17][C:3]=1[N:4]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]>CO.[Pd]>[F:1][C:2]1[CH:20]=[C:19]([NH2:21])[CH:18]=[CH:17][C:3]=1[N:4]([CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 900241452-fluoro-N,N-di-n-hexyl-4-nitroaniline

생성물 1

HCID 117966053HCID 117966053, 화합물수율 63%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To a solution of 2-fluoro-N,N-di-n-hexyl-4-nitroaniline (2.79 g, 8.64 mmol) in MeOH (50 mL) was added catalyst Pd/C (0.28 g). The reaction mixture was stirred at rt under H2 overnight, and filtered. The filtrate was concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=10:1) to give the title compound as pale yellow oil (1.60 g, 63%).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • filtrationfiltered
  • concentrationThe filtrate was concentrated in vacuo
  • customThe residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=10:1)
  • 출처 및 근거

    ORD 기록
    ord-1e3514b894634a49afe3431ddff5b933
    출처 데이터셋
    uspto-grants-2016_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09434695B2

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