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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 24335생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/24335

반응식

참여 물질

역할이름HCID투입량
반응물(2-(Dimethylamino)ethyl)triphenylphosphonium bromideHCID 2724136—
반응물ethyl 3-formyl-1H-indole-2-carboxylateHCID 5107764—
반응물Lithium diethylamineHCID 45051810—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물3-(3-dimethylaminopropenyl)-1H-indole-2-carboxylic acid ethyl esterHCID 54356828—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06855730B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-bef9feba2e844741aa8e3640f2b05a5a
출처 메모uspto-grants-2005_02