反応式
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([Br:12])[CH:8]=2)[N:3]=1.[CH3:13][O-:14].[Na+]>CO>[Br:12][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([O:14][CH3:13])[CH:11]=[CH:10]2参加物
4
実験手順
A solution of 2-chloro-6-bromoquinoline (4.0 g) in methanol (20 cm3) was heated under reflux with sodium methoxide [made from sodium (0.5 g) and methanol (20 cm3)] for 16 hours. The solvent was removed in vacuo and the residue was partitioned, between water (20 cm3) and chloroform (100 cm3). The aqueous phase was extracted wth chloroform (2×30 cm3) and the dried (MgSO4) organic extracts were evaporated to give a solid which was recrystallised from petroleum ether (b.p. 60°-80°) to yield the title compound, m.p. 93°-96°, (3.0 g).
後処理
- customThe solvent was removed in vacuo
- customthe residue was partitioned, between water (20 cm3) and chloroform (100 cm3)
- extractionThe aqueous phase was extracted wth chloroform (2×30 cm3)
- dry with materialthe dried (MgSO4) organic extracts
- customwere evaporated
- customto give a solid which
- customwas recrystallised from petroleum ether (b.p. 60°-80°)
出典と根拠
- ORDレコード
- ord-80bb0d7044fe4160bd24da6454bc31de
- 出典データセット
- uspto-grants-1988_03
- 特許番号
- US04728654
関連ノート
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