반응식
C[O:2][C:3]1[CH:8]=[C:7]([CH2:9][CH2:10][CH3:11])[CH:6]=[CH:5][C:4]=1[O:12][C:13]1[CH:18]=[CH:17][C:16]([O:19][CH3:20])=[CH:15][CH:14]=1.B(Br)(Br)Br>>[CH3:20][O:19][C:16]1[CH:17]=[CH:18][C:13]([O:12][C:4]2[CH:5]=[CH:6][C:7]([CH2:9][CH2:10][CH3:11])=[CH:8][C:3]=2[OH:2])=[CH:14][CH:15]=1참가 물질
3
실험 절차
According to the procedure of example 5(b) except substituting 2-fluoro-6-(2-methoxy-4-propylphenoxy)pyridine for 2-methoxy-1-(4-methoxyphenoxy)-4-propylbenzene (0.18 mmol; 50 mg) and adding 4 equivalents (0.735 mmol; 735 μl) of boron tribromide, the title compound was prepared in 32% yield (0.06 mmol; 15 mg) after purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—20/80).
후처리
- customafter purification by preparative TLC on silica gel (ethyl acetate/cyclohexane—20/80)
출처 및 근거
- ORD 기록
- ord-c54a8973bc1b45e39e7e78dc6e8b723f
- 출처 데이터셋
- uspto-grants-2014_05
- 특허 번호
- US08722746B2
연결된 노트
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