Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725360Generated: November 1, 2026

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

https://huagongshe.com/reaction/1725360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndole-7-carboxaldehydeHCID 2734629—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product7-Ethenyl-1H-indoleHCID 14567404—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07491716B2
Source datasetuspto-grants-2009_02
ORD IDord-2ed36e5f038341deb500a2476631da61
Source noteuspto-grants-2009_02