戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 641894作成日:2026年10月25日

m-Chloroperbenzoic acid → HCID 49758908、化合物

https://huagongshe.com/reaction/641894

反応式

関与物質

役割名称HCID仕込み量
反応物m-Chloroperbenzoic acidHCID 70297—
反応物1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carbaldehydeHCID 10356646—
溶媒DichloromethaneHCID 6344—
生成物HCID 49758908HCID 49758908—

反応条件

温度0 °C

反応手順

Into a 250 mL 3-necked round bottom flask was placed dichloromethane (30 mL). To the mixture was added mCPBA (m-chloroperbenzoic acid) (2.78 g, 13.69 mmol), while cooling to a temperature of 0° C. This was followed by the addition of a solution of 1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carbaldehyde (3 g, 10.49 mmol) in dichloromethane (100 mL), which was added dropwise with stirring, while cooling to a temperature of 0° C. The resulting solution was allowed to react, with stirring, 2 hours while the temperature was maintained at 0° C. Then the resulting solution was allowed to react, with stirring, overnight while the temperature was maintained at 30° C. in a bath of oil. The reaction progress was monitored by LC-MS. The residue was purified by eluting through a column with a 1:10 ethyl acetate/petroleum ether solvent system. This resulted in 2 g (63%) of 1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-3-yl formate as a light yellow solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07696229B2
出典データセットuspto-grants-2010_04
ORD IDord-a6a0fae6c8f64b7cbac1fa18c0c15ddf
出典メモuspto-grants-2010_04