Bromine → 2-Bromo-7-nitro-3,4-dihydronaphthalen-1(2H)-one
反応式
[N+:1]([C:4]1[CH:13]=[C:12]2[C:7]([CH2:8][CH2:9][CH2:10][C:11]2=[O:14])=[CH:6][CH:5]=1)([O-:3])=[O:2].[Br:15]Br>CCOCC>[Br:15][CH:10]1[CH2:9][CH2:8][C:7]2[C:12](=[CH:13][C:4]([N+:1]([O-:3])=[O:2])=[CH:5][CH:6]=2)[C:11]1=[O:14]参加物
4
実験手順
To a suspension of 9.56 g (0.05 mol) of 7-nitro-1-tetralone in 250 mL of ether was added bromine dropwise. The progress of the reaction was followed by thin layer chromatography (fl. silica gel/CH2Cl2). When all of the starting material had been consumed, the mixture was concentrated and cyclohexane was added. The white solid was removed by filtration to afford 2.25 g of 2-bromo-7-nitrotetralone, mp 94°-96° C.
後処理
- customWhen all of the starting material had been consumed
- concentrationthe mixture was concentrated
- additioncyclohexane was added
- customThe white solid was removed by filtration
出典と根拠
- ORDレコード
- ord-d3ed7897c4024e418d5b32db5db3219e
- 出典データセット
- uspto-grants-1991_07
- 特許番号
- US05032598
反応ノート
読み込み中…