Cesium carbonate → 1,3-Dibromo-5-monofluoromethoxybenzene
반응식
[Br:1][C:2]1[CH:3]=[C:4]([OH:9])[CH:5]=[C:6]([Br:8])[CH:7]=1.C([O-])([O-])=O.[Cs+].[Cs+].Cl[CH2:17][F:18]>CN(C=O)C.O>[Br:1][C:2]1[CH:3]=[C:4]([O:9][CH2:17][F:18])[CH:5]=[C:6]([Br:8])[CH:7]=1참가 물질
실험 절차
To a tared, sealed 350 mL round-bottomed pressure flask containing a suspension of 3,5-dibromophenol (10.0 g, 39.7 mmol; see step (ii) above) and Cs2CO3 (20.7 g, 63.5 mmol) in DMF (150 mL) at −78° C. was added chlorofluoromethane via bubbling for 5 min through the septum. The septum was replaced with a Teflon stopper and the flask was then sealed and allowed to warm to room temperature where the flask was weighed and determined to contain 9.0 g (131 mmol) of chlorofluoromethane. The solution was heated in an oil bath set at 70° C. overnight. The flask was cooled to room temperature, the pressure cautiously released and the contents diluted with water (100 mL). The aqueous layer was extracted with Et2O (3×200 mL) then, the combined organics were dried (Na2SO4), filtered and concentrated in vacuo. Flash chromatography on silica gel eluting with hexanes afforded the sub-title compound (7.9 g, 71%) as a white solid.
후처리
- customsealed 350 mL round-bottomed pressure flask
- additioncontaining
- customvia bubbling for 5 min through the septum
- customthe flask was then sealed
- temperatureThe solution was heated in an oil bath
- temperatureThe flask was cooled to room temperature
- extractionThe aqueous layer was extracted with Et2O (3×200 mL)
- dry with materialthe combined organics were dried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-62c1e88e2a3d4ac7a49537d206b553ec
- 출처 데이터셋
- uspto-grants-2010_09
- 특허 번호
- US07803954B2
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