Potassium Carbonate → 1-Bromo-3,5-dichloro-2-(2,2-difluoroethoxy)benzene

HRID 1404552노트

반응식

HRID 1404552 반응식
[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[OH:10].C([O-])([O-])=O.[K+].[K+].[F:17][CH:18]([F:25])[CH2:19]OS(C)(=O)=O>CN(C=O)C>[Br:1][C:2]1[CH:7]=[C:6]([Cl:8])[CH:5]=[C:4]([Cl:9])[C:3]=1[O:10][CH2:19][CH:18]([F:25])[F:17]

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 206172-Bromo-4,6-dichlorophenolHCID 567764922,2-Difluoroethyl methanesulfonate

생성물 1

HCID 441966871-Bromo-3,5-dichloro-2-(2,2-difluoroethoxy)benzene

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of 2-bromo-4,6-dichloro-phenol (14.6 g, 60.3 mmol, Step A compound) in DMF (10 ml) were added K2CO3 (16.53 g, 120.6 mmol) and methanesulfonic acid 2,2-difluoro-ethyl ester (10.7 g, 66.4 mmol, Step B compound) and the mixture was heated to reflux for 16 h. The DMF was then evaporated in vacuo and the resulting residue was dissolved in EtOAc (300 ml). This solution was washed two times with water, with brine, dried with Na2SO4 and evaporated. The remaining crude product was purified by chromatography (silica gel; hexane) and the title compound was obtained as white solid (14.5 g, 79%). MS: m/z=304 [M]+.

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 16 h
  3. customThe DMF was then evaporated in vacuo
  4. dissolutionthe resulting residue was dissolved in EtOAc (300 ml)
  5. washThis solution was washed two times with water
  6. dry with materialwith brine, dried with Na2SO4
  7. customevaporated
  8. customThe remaining crude product was purified by chromatography (silica gel; hexane)

출처 및 근거

ORD 기록
ord-e1732f944139462abea642e77db66850
출처 데이터셋
uspto-grants-2014_12
특허 번호
US08912221B2

반응 노트

불러오는 중…