戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1989265作成日:2026年10月27日

Thionyl Chloride → 3-[6'-Methyl-4'-(4-trifluoromethyl-phenyl)-[2,2']bipyridinyl-6-yl]-benzenesulfonyl chloride

https://huagongshe.com/reaction/1989265

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物Sodium BicarbonateHCID 516892—
反応物3-[6'-Methyl-4'-(4-trifluoromethyl-phenyl)-[2,2']bipyridinyl-6-yl]-benzenesulfonic acidHCID 16747649—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物3-[6'-Methyl-4'-(4-trifluoromethyl-phenyl)-[2,2']bipyridinyl-6-yl]-benzenesulfonyl chlorideHCID 86615450—

反応条件

温度23 °C

反応手順

To a suspension of 3-[6′-methyl-4′-(4-trifluoromethyl-phenyl)-[2,2′]bipyridinyl-6-yl]-benzenesulfonic acid (example 345) (2.0 g, 4.25 mmol) in DMF (20 mL) at 23° C. was added thionyl chloride (1.54 mL, 21.25 mmol) and the mixture was stirred at 23° C. for 2 h, then added again SOCl2 (1.54 mL, 21.25 mmol) and the mixture was stirred at 23° C. for 1 h. Diluted with EtOAc, poured into ice cold half-sat. NaHCO3-sol., separated phases, washed organic layer with brine and dried over Na2SO4. Removal of the solvent in vacuum left the title compound as an off-white solid (2.0 g, 98%), which was used without further purification. MS (ISP) 489.2 [(M+H)+] and 491.1 [(M+2+H)+].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07642264B2
出典データセットuspto-grants-2010_01
ORD IDord-96384423d5e542ef979aaecb75114cdf
出典メモuspto-grants-2010_01