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HRID 522589作成日:2026年10月26日

Benzenesulfonyl chloride → 1-(Phenylsulfonyl)-3-indolecarboxaldehyde

https://huagongshe.com/reaction/522589

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonyl chlorideHCID 7369—
反応物Indole-3-CarboxaldehydeHCID 10256—
反応物Potassium HydroxideHCID 14797—
溶媒EthanolHCID 702—
生成物1-(Phenylsulfonyl)-3-indolecarboxaldehydeHCID 36333433%

反応手順

To a solution of indole 3-carboxaldehyde (8y) (100 mmol) in ethanol (500 mL) at RT was added potassium hydroxide (1.1 equiv). The mixture was stirred until total solubilization. The ethanol was completely removed in vacuum and the residual was dissolved in acetone (250 mL) followed by adding benzenesulfonyl chloride (1.1 equiv, 110 mmol). The reaction mixture was stirred for half hour. The precipitate was filtered off and the filtrate was concentrated and recrystallized from methanol to give a white solid. Yield: 33%. 1H NMR (500 MHz, CDCl3) δ 10.17 (s, 1H), 8.25-8.39 (m, 2H), 7.97-8.09 (m, 3H), 7.69 (t, J=7.33 Hz, 1H), 7.59 (t, J=7.5 Hz, 2H), 7.39-7.54 (m, 2H). MS (ESI) calcd for C15H11NO3S 285.1. Found 286.0 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09334242B2
出典データセットuspto-grants-2016_05
ORD IDord-b3baf7e1a78044428172788db1013774
出典メモuspto-grants-2016_05