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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 351588Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/351588

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

To a solution of methyl triphenylphosphonium bromide (5.05 g, 14.1 mmol) in tetrahydrofuran (80 mL) was added potassium tert-butoxide (1 M in tetrahydrofuran, 14.1 mL, 14.1 mmol) and the reaction stirred for 45 minutes at room temperature. Next a prepared solution of 7-formylindole (1.00 g, 6.89 mmol) in tetrahydrofuran (10 mL) was added and the reaction stirred for 1.5 hours. The reaction mixture was diluted with ethyl acetate (250 mL) and washed with an 8:1 mixture of water and 1 N hydrochloric acid (2×100 mL), saturated aqueous sodium chloride (100 mL), and dried over sodium sulfate. The solution was filtered and the filtrate concentrated under reduced pressure. The residue was subjected to silica gel chromatography. Fractions containing product were combined and concentrated under reduced pressure to provide the desired compound as a brown oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06743785B2
Quelldatensatzuspto-grants-2004_06
ORD IDord-43a1ca3d2ecd4c47834d89a23cb06795
Quellennotizuspto-grants-2004_06