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HRID 1198562作成日:2026年10月27日

Potassium Carbonate → 7-(Cyanomethoxy)indole

https://huagongshe.com/reaction/1198562

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物BromoacetonitrileHCID 11534—
反応物trans-3-[2-(7-Chloroquinolin-2-yl)ethenyl]benzyl alcoholHCID 10827738—
触媒Palladium hydroxideHCID 9942167—
溶媒MethanolHCID 887—
溶媒TolueneHCID 1140—
生成物7-(Cyanomethoxy)indoleHCID 15054020—

反応手順

The protected 7-substituted indole (Example 34a part ii) (0.53 g, 1.75 mmol) in methanol (10 ml) and toluene (10 ml) was hydrogenated in a Parr apparatus at 50 p.s.i. for 1 hour in the presence of Pearlman's catalyst (0.33 g). The reaction mixture was filtered through Celite and the filtrate evaporated in vacuo. The crude 7-hydroxy indole was taken up in methyl ethyl ketone (20 ml), and bromoacetonitrile (0.65 g, 5.25 mmol) and anhydrous potassium carbonate (0.6 g, 4.35 mmol) added. The mixture was refluxed under nitrogen for 1 hour, cooled, poured into 2.5M hydrochloric acid/ice and extracted into dichloromethane. The organic phase was washed with water, dried, filtered and evaporated in vacuo.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05281593
出典データセットuspto-grants-1994_01
ORD IDord-cfb28e7ed3b24622adf9dc9b1f6170ad
出典メモuspto-grants-1994_01