戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 41534作成日:2026年10月23日

1-(4-Methylbenzene-1-sulfonyl)-1H-indole-3-carbaldehyde → (1-tosyl-1H-indol-3-yl)methanol

https://huagongshe.com/ja/reaction/41534

反応式

関与物質

役割名称HCID仕込み量
反応物1-(4-Methylbenzene-1-sulfonyl)-1H-indole-3-carbaldehydeHCID 735817—
反応物Sodium borohydrideHCID 4311764—
溶媒MethanolHCID 887—
生成物(1-tosyl-1H-indol-3-yl)methanolHCID 83926392.2%

反応手順

To a solution of 1-tosyl-1H-indole-3-carbaldehyde (7 g, 23.385 mmol) in MeOH (70 mL), NaBH4 (1.77 g, 46.769 mmol) was added at 0° C. and the mixture was stirred for 10 min. The reaction mixture was allowed to warm to rt and stirring was continued for 18 h. The solvent was removed under reduced pressure at 45° C. and the crude reaction mixture was quenched with saturated aqueous ammonium chloride solution. Ethyl acetate was added and the organic layer was washed with water and brine. The organic layer was dried over anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure to yield a solid (6.5 g, 92%). [1H-NMR (CDCl3, 300 MHz) δ 8.02-7.95 (m, 1H), 7.82-7.75 (m, 2H), 7.65-7.53 (m, 2H), 7.40-7.19 (m, 4H)].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530648B2
出典データセットuspto-grants-2013_09
ORD IDord-13947a147af8496a8baa8ac63ebdbe9e
出典メモuspto-grants-2013_09