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3-(Trifluoromethyl)phenol → 1-(4-Nitrophenoxy)-3-(trifluoromethyl)benzene

HRID 1824691
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인쇄 미리보기

반응식

HRID 1824691 반응식
Cl[C:2]1[CH:7]=[CH:6][C:5]([N+:8]([O-:10])=[O:9])=[CH:4][CH:3]=1.[F:11][C:12]([F:21])([F:20])[C:13]1[CH:14]=[C:15]([OH:19])[CH:16]=[CH:17][CH:18]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[N+:8]([C:5]1[CH:6]=[CH:7][C:2]([O:19][C:15]2[CH:16]=[CH:17][CH:18]=[C:13]([C:12]([F:11])([F:20])[F:21])[CH:14]=2)=[CH:3][CH:4]=1)([O-:10])=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 73763-(Trifluoromethyl)phenolHCID 74741-Chloro-4-nitrobenzeneHCID 11430Potassium Carbonate

생성물 1

HCID 2433091-(4-Nitrophenoxy)-3-(trifluoromethyl)benzene

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
120 °C

실험 절차

A mixture of 1-chloro-4-nitrobenzene (11 g), 3-(trifluoromethyl)phenol (12 g), and potassium carbonate (21 g) in dimethyl formamide (175 mL) was heated at 120° C. for about 16 hours. The reaction mixture was cooled to room temperature and poured over ice-water. The mixture was filtered and the solid collected was washed with water and dried under vacuum (25 g).

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. filtrationThe mixture was filtered
  3. customthe solid collected
  4. washwas washed with water
  5. customdried under vacuum (25 g)

출처 및 근거

ORD 기록
ord-1a62947be93f4dfd997a416185903f5e
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07045512B2

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