N-bromobutanimide → 3,6-Dibromoisobenzofuran-1(3H)-one
反応式
[Br:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][O:7][C:8]2=[O:9])=[CH:4][CH:3]=1.[Br:12]N1C(=O)CCC1=O.N(CCCC#N)=NCCCC#N>C(Cl)(Cl)(Cl)Cl>[Br:12][CH:6]1[C:5]2[C:10](=[CH:11][C:2]([Br:1])=[CH:3][CH:4]=2)[C:8](=[O:9])[O:7]1参加物
5
実験手順
6-Bromophthalide (5.85 gms; 0.0275 mole), N-bromosuccinimide (4.89 gm; 0.0275 mole) and azobisbutyronitrile (0.1 gm) were gently refluxed in dry carbon tetrachloride (200 ml.) for 2 hours. On cooling, the succinimide was filtered off and the solvent removed in vacuo to give an oil, which was used immediately.
後処理
- temperatureOn cooling
- filtrationthe succinimide was filtered off
- customthe solvent removed in vacuo
- customto give an oil, which
出典と根拠
- ORDレコード
- ord-23a4df72807d4b6487d6dc5c09f1fc0c
- 出典データセット
- uspto-grants-1977_07
- 特許番号
- US04036829
反応ノート
読み込み中…