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Benzene → Tetraethylammonium 4-Nitrophenolate

HRID 280360
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인쇄 미리보기

반응식

HRID 280360 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[CH:6][CH:5]=1)([O-:3])=[O:2].C1C=CC=CC=1.[OH-].[CH2:18]([N+:20]([CH2:25][CH3:26])([CH2:23][CH3:24])[CH2:21][CH3:22])[CH3:19]>O>[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([O-:10])=[CH:6][CH:5]=1)([O-:3])=[O:2].[CH2:18]([N+:20]([CH2:25][CH3:26])([CH2:23][CH3:24])[CH2:21][CH3:22])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 241BenzeneHCID 9804-NitrophenolHCID 6509Tetraethylammonium Hydroxide

생성물 1

HCID 23322207Tetraethylammonium 4-Nitrophenolate수율 94.7%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of 4-nitrophenol (13.9 g, 0.10 mol) and benzene (250 mL) was treated with tetraethylammonium hydroxide (14.7 g, 0.10 mol), added as a 20% aqueous solution. The mixture was heated under reflux until all water was removed by azeotropic distillation. The solution was allowed to cool with continued stirring. Upon standing, 25.4 g of a yellow solid was obtained; it was recrystallized from THF. 1H NMR (CDCl3) confirmed the title compound.

후처리

  1. temperatureThe mixture was heated
  2. customwas removed by azeotropic distillation
  3. temperatureto cool with continued stirring

출처 및 근거

ORD 기록
ord-ee8ea755095f40dfa79c74726b8d381f
출처 데이터셋
uspto-grants-1986_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04588795

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