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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 557163Erstellt: 25. Oktober 2026

Indole-7-carboxaldehyde → 7-Ethenyl-1H-indole

https://huagongshe.com/reaction/557163

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIndole-7-carboxaldehydeHCID 2734629—
EduktPotassium tert-butoxideHCID 23665647—
KatalysatorMethyltriphenyliphosphonium bromideHCID 74505—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt7-Ethenyl-1H-indoleHCID 14567404—

Reaktionsschritte

Add potassium tert-butoxide (1 M in tetrahydrofuran, 14.1 mL, 14.1 mmol) to a solution of methyl triphenylphosphonium bromide (5.05 g, 14.1 mmol) in tetrahydrofuran (80 mL) and stir the reaction mixture for 45 minutes at room temperature. Add a solution of 7-formylindole (1.00 g, 6.89 mmol) in tetrahydrofuran (10 mL) and stirred for 1.5 hours. Dilute the reaction mixture with ethyl acetate (250 mL), wash sequentially with an 8:1 mixture of water and 1 N hydrochloric acid (2×100 mL) and saturated aqueous sodium chloride (100 mL), dry over sodium sulfate, filter, and concentrate the filtrate under reduced pressure. Subject the residue silica gel chromatography. Combine fractions containing product and concentrate them under reduced pressure to provide the desired compound as a brown oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08058425B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-26848bd307884ed187f181d62ab4656b
Quellennotizuspto-grants-2011_11