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2,6-Dichlorophenol → Phenol, 2,6-dichloro-4-fluoro-

HRID 1197127
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인쇄 미리보기

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HRID 1197127 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[OH:9].[F:10][N+]1C(C(Cl)(Cl)Cl)=CC=CC=1Cl>ClC(Cl)CCl>[F:10][C:6]1[CH:7]=[C:2]([Cl:1])[C:3]([OH:9])=[C:4]([Cl:8])[CH:5]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 68992,6-DichlorophenolHCID 11078230N-fluoro-2-chloro-6-(trichloromethyl) pyridinium

생성물 1

HCID 94950Phenol, 2,6-dichloro-4-fluoro-

시약·촉매·용매 1

HCID 65741,1,2-Trichloroethane용매

반응 조건

온도
55 °C

실험 절차

A mixture of 082 g of 2,6-dichlorophenol, 1.67 g of N-fluoro-2-chloro-6-(trichloromethyl) pyridinium rfluoroborate, and 40 ml of 1,1,2-trichloroethane was placed in a 100 ml 3-necked round bottomed flask equipped with a magnetic stirring bar, a thermometer, and a reflux condenser. The mixture was heated to 55° C. and allowed to react at that temperature for 8 hours under nitrogen. The mixture was then allowed to cool. Analysis by standardized gas-liquid chromatography using a mass spectrometer detector indicated that the title product was present in 24 percent conversion. The product identity was confirmed by its known 19F and 1H NMR spectra.

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후처리

  1. customwas placed in a 100 ml 3-necked round bottomed flask
  2. customequipped with a magnetic stirring bar
  3. customto react at that temperature for 8 hours under nitrogen
  4. temperatureto cool

출처 및 근거

ORD 기록
ord-452532e5bdb94482bb2780cdd21dd7f2
출처 데이터셋
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05116982

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