Azobisisobutyronitrile → HCID 89996156、化合物
反応式
[Cl:1][C:2]1[N:7]=[C:6]([CH3:8])[C:5]([I:9])=[CH:4][CH:3]=1.C1C(=O)N([Br:17])C(=O)C1.CC(N=NC(C#N)(C)C)(C#N)C>ClCCCl>[Br:17][CH2:8][C:6]1[C:5]([I:9])=[CH:4][CH:3]=[C:2]([Cl:1])[N:7]=1参加物
5
反応条件
- 温度
- 80 °C
実験手順
To a stirred solution of 6-chloro-3-iodo-2-methyl-pyridine (20 g, 79 mmol, 1 eq) in 1,2-dichloroethane (200 mL) was added NBS (21.1 g, 118.6 mmol, 1.5 eq) followed by addition of AIBN (5.2 g, 31.6 mmol, 0.4 eq) at room temperature in dark. Resulting reaction mixture was heated at 80° C. for 16 hours. After maximum consumption of starting material, reaction mixture was cooled to room temperature and quenched with water (50 mL), extracted with DCM (3×50 mL). Combined organic phase was washed with brine (50 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure to get dark brown semi solid (20 g, crude). Crude of title compound was used as such for next reaction. 1H NMR not clean. LC-MS: No ionization.
後処理
- customResulting
- customreaction mixture
- customAfter maximum consumption of starting material, reaction mixture
- temperaturewas cooled to room temperature
- customquenched with water (50 mL)
- extractionextracted with DCM (3×50 mL)
- washCombined organic phase was washed with brine (50 mL)
- dry with materialdried over anhydrous Na2SO4
- concentrationconcentrated under reduced pressure
- customto get dark brown semi solid (20 g, crude)
出典と根拠
- ORDレコード
- ord-2bf8c7ac00fd437e9b1e663013b2c937
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09131697B2
反応ノート
読み込み中…