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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351588Generated: October 25, 2026

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

https://huagongshe.com/reaction/351588

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

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743785B2
Source datasetuspto-grants-2004_06
ORD IDord-43a1ca3d2ecd4c47834d89a23cb06795
Source noteuspto-grants-2004_06