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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Indole-7-carboxaldehyde | HCID 2734629 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-Ethenyl-1H-indole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06743785B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-43a1ca3d2ecd4c47834d89a23cb06795 |
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| Source note | uspto-grants-2004_06 |
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