反応式
[CH3:1][C:2]1[N:12]=[CH:11][CH:10]=[CH:9][C:3]=1[C:4]([O:6][CH2:7][CH3:8])=[O:5].[Br:13]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.C(Cl)(Cl)(Cl)[Cl:40]>>[ClH:40].[CH2:7]([O:6][C:4]([C:3]1[C:2]([CH2:1][Br:13])=[N:12][CH:11]=[CH:10][CH:9]=1)=[O:5])[CH3:8]参加物
5
実験手順
A mixture of ethyl 2-methylnicotinate (5.0 g, 30.3 mmol), N-bromosuccinimide (7.5 g, 42.1 mmol) and benzoyl peroxide (0.5 g) in carbon tetrachloride (100 ml) was heated under reflux for 6 hours, then allowed to cool. The resulting mixture was filtered, the filtered solid washed with carbon tetrachloride, and the combined filtrate washed with 4% sodium hydroxide solution, water and 2% hydrochloric acid, then dried over sodium sulphate. The solution was then treated with ethereal hydrochloric acid, and the resulting precipitate was filtered off, washed with ether and dried to afford the title compound as a pale yellow solid (4.5 g).
後処理
- temperaturewas heated
- temperatureunder reflux for 6 hours
- temperatureto cool
- filtrationThe resulting mixture was filtered
- washthe filtered solid washed with carbon tetrachloride
- washthe combined filtrate washed with 4% sodium hydroxide solution, water and 2% hydrochloric acid
- dry with materialdried over sodium sulphate
- additionThe solution was then treated with ethereal hydrochloric acid
- filtrationthe resulting precipitate was filtered off
- washwashed with ether
- customdried
出典と根拠
- ORDレコード
- ord-7ba493fbd2a4497ea6459bdf9bba5351
- 出典データセット
- uspto-grants-2005_08
- 特許番号
- US06933312B2
関連ノート
読み込み中…