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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 24335Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/24335

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(2-(Dimethylamino)ethyl)triphenylphosphonium bromideHCID 2724136—
Eduktethyl 3-formyl-1H-indole-2-carboxylateHCID 5107764—
EduktLithium diethylamineHCID 45051810—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-(3-dimethylaminopropenyl)-1H-indole-2-carboxylic acid ethyl esterHCID 54356828—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06855730B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-bef9feba2e844741aa8e3640f2b05a5a
Quellennotizuspto-grants-2005_02