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HRID 1399478作成日:2026年10月26日

Potassium Hydroxide → N-(5-carboxypentyl)-3-(1-naphthoyl)-1H-indole

https://huagongshe.com/reaction/1399478

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物N-(5-Ethoxycarbonylpentyl)-3-(1-naphthoyl)-1H-indoleHCID 68159362—
溶媒Oxolane--water (1/1)HCID 21881883—
生成物N-(5-carboxypentyl)-3-(1-naphthoyl)-1H-indoleHCID 68159208—

反応条件

温度60 °C

反応手順

To a solution of 2 (5.0 g, 12 mmol) in a mixture of THF/H2O (1:1) was added potassium hydroxide (1.7 g) and the mixture was stirred at 60° C. for 1 h. The THF was removed under vacuum, the aqueous solution acidified to pH 1 by the addition of hydrochloric acid solution (1N) and extracted by ethyl acetate (3×100 ml). The combined organic phases were washed by water (100 ml), brine solution (100 ml), dried over sodium sulphate, filtered and concentrated to dryness. The crude product obtained was dissolved in ethyl acetate (10 ml) and the Hapten-A precipitated by the addition of a mixture of ether/hexane as a white solid, filtered and dried under high vacuum to give Hapten-A (3.6 g, 78%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08906633B2
出典データセットuspto-grants-2014_12
ORD IDord-ed42053bc5004595b27cdb683a5a48c7
出典メモuspto-grants-2014_12