Boron tribromide → 2-(3-Hydroxyphenyl)quinolin-6-ol
反応式
C[O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]=[C:8]([C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([O:19]C)[CH:14]=1)[CH:7]=[CH:6]2.B(Br)(Br)Br>>[OH:19][C:15]1[CH:14]=[C:13]([C:8]2[CH:7]=[CH:6][C:5]3[C:10](=[CH:11][CH:12]=[C:3]([OH:2])[CH:4]=3)[N:9]=2)[CH:18]=[CH:17][CH:16]=1参加物
3
実験手順
The compound is prepared by reaction of 6-methoxy-2-(3-methoxyphenyl)quinoline (77 mg, 0.29 mmol, 1 eq) with boron tribromide (15 eq) according to method G. Purification by column chromatography with hexane/ethyl acetate 7/3 as the eluent yields the desired product in a yield of 10%, 7 mg.
後処理
- customPurification by column chromatography with hexane/ethyl acetate 7/3 as the eluent
出典と根拠
- ORDレコード
- ord-dcdb294dd069481abc4d45da19ed107c
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08546392B2
反応ノート
読み込み中…