反応式
[Br:1]N1C(=O)CCC1=O.C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.[Cl:27][C:28]1[CH:33]=[CH:32][C:31]([CH3:34])=[CH:30][N:29]=1.O>C(Cl)(Cl)(Cl)Cl>[Br:1][CH2:34][C:31]1[CH:32]=[CH:33][C:28]([Cl:27])=[N:29][CH:30]=1参加物
6
実験手順
N-bromosuccinimide (6.1 g, 3.44 mmol) and benzoyl peroxide (218 mg, 0.09 mmol) were added successively to a solution of 2-chloro-5-methyl-pyridine (4.0 g, 3.13 mmol) in carbon tetrachloride (20 mL) and refluxed for 90 min. The reaction mixture was cooled to room temperature, water added and the organic layer separated. The organic layer was washed successively with water, brine, dried over anhydrous sodium sulfate and filtered. The resultant solution of 5-bromomethyl-2-chloro-pyridine was used as such for the next step.
後処理
- temperaturerefluxed for 90 min
- customthe organic layer separated
- washThe organic layer was washed successively with water, brine
- dry with materialdried over anhydrous sodium sulfate
- filtrationfiltered
出典と根拠
- ORDレコード
- ord-19f91466f0b74cba80a0973a69dea6d8
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08524705B2
関連ノート
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