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HRID 24335作成日:2026年10月26日

(2-(Dimethylamino)ethyl)triphenylphosphonium bromide → 3-(3-dimethylaminopropenyl)-1H-indole-2-carboxylic acid ethyl ester

https://huagongshe.com/reaction/24335

反応式

関与物質

役割名称HCID仕込み量
反応物(2-(Dimethylamino)ethyl)triphenylphosphonium bromideHCID 2724136—
反応物ethyl 3-formyl-1H-indole-2-carboxylateHCID 5107764—
反応物Lithium diethylamineHCID 45051810—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物3-(3-dimethylaminopropenyl)-1H-indole-2-carboxylic acid ethyl esterHCID 54356828—

反応手順

Butyllithium (1.1 equiv.) was added to a suspension of (2-dimethylaminoethyl)triphenylphosphonium bromide in THF (0.2 M) at 0° C. After stirring for 30 minutes, lithium diethylamine (1.1 equiv.) was added dropwise followed by the cold suspension of 3-formyl-1H-indole-2-carboxylic acid ethyl ester (3.96 g, 18.2 mmol) in THF. The resulting orange suspension was stirred for 18 hours. The reaction was then quenched with saturated ammonium chloride and extracted with 10% MeOH in DCM. The organic layer was washed with saturated sodium bicarbonate, dried and concentrated to give 3-(3-dimethylaminopropenyl)-1H-indole-2-carboxylic acid ethyl ester as a brownish-red waxy solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855730B2
出典データセットuspto-grants-2005_02
ORD IDord-bef9feba2e844741aa8e3640f2b05a5a
出典メモuspto-grants-2005_02