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1-(3-Fluorobenzyloxy)-2-methyl-4-nitrobenzene → 3-Methyl-4-[(3-fluorobenzyl)oxy]aniline

HRID 550413
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인쇄 미리보기

반응식

HRID 550413 반응식
[F:1][C:2]1[CH:3]=[C:4]([CH:17]=[CH:18][CH:19]=1)[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-])=O)=[CH:9][C:8]=1[CH3:16].[H][H]>C(O)C.O=[Pt]=O>[CH3:16][C:8]1[CH:9]=[C:10]([CH:11]=[CH:12][C:7]=1[O:6][CH2:5][C:4]1[CH:17]=[CH:18][CH:19]=[C:2]([F:1])[CH:3]=1)[NH2:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 221379601-(3-Fluorobenzyloxy)-2-methyl-4-nitrobenzeneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 221379333-Methyl-4-[(3-fluorobenzyl)oxy]aniline수율 100.3%

시약·촉매·용매 2

HCID 345198Adams' catalyst촉매HCID 702Ethanol용매

실험 절차

A mixture of 1-[(3-fluorobenzyl)oxy]-2-methyl-4-nitrobenzene (3.2 g, 12.2 mmol) and PtO2 (320 mg) in ethanol (250 ml) was stirred under an atmosphere of hydrogen (1.2 bar) until completion of the reaction (the reaction being complete when 3 mole equivalents of hydrogen have been reacted). The mixture was then filtered over celite and the solvent evaporated to give 3-methyl-4-[(3-fluorobenzyl)oxy]aniline as a yellow oil (2.83 g, 100%);

후처리

  1. customhave been reacted)
  2. filtrationThe mixture was then filtered over celite
  3. customthe solvent evaporated

출처 및 근거

ORD 기록
ord-9efa0effb77745d5a0f2f7e81f956d62
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07947676B2

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