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HRID 1865作成日:2026年10月23日

Azobisisobutyronitrile → 4-Chloro-5-fluoro-alpha-bromo-2-picoline

https://huagongshe.com/ja/reaction/1865

反応式

関与物質

役割名称HCID仕込み量
反応物AzobisisobutyronitrileHCID 6547—
反応物N-bromobutanimideHCID 67184—
反応物4-Chloro-5-fluoro-2-methylpyridineHCID 19691410—
溶媒1,2-DichloroethaneHCID 11—
溶媒DichloromethaneHCID 6344—
生成物4-Chloro-5-fluoro-alpha-bromo-2-picolineHCID 8675004269%

反応条件

温度75 °C

反応手順

4-Chloro-5-fluoro-2-picoline (2.9 g, 20 mmol), the product of Example 66, was dissolved in 50 mL of 1,2-dichloroethane in a dry flask. The resultant solution was heated, with stirring, to 75° C. and 4.09 (23 mmol) of N-bromosuccinimide was added, followed by 100 mG (0.7 mmol) of 2,2-azobisisobutyronirile (AIBN), a free radical initiator. After the reaction mixture was stirred at 75° C. for 24 hours, it was diluted with 450 mL of methylene chloride and washed with 3 X 400 mL of water. The organic layer was separated and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was dried in vacuo to give 3.5 g (69% yield) of the title compound as an amber oil; 1H NMR (CDCl3) d 4.50 (s, 2H), 7.54 (d, 1H), 8.44 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726182
出典データセットuspto-grants-1998_03
ORD IDord-b9b54b14eaa34567839b3bc713494b14
出典メモuspto-grants-1998_03