HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910064Generated: October 30, 2026
Indole-7-carboxaldehyde → 7-Ethenyl-1H-indole
https://huagongshe.com/reaction/910064
Participants
| Role | Name | HCID | Charge |
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| 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
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022065B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-2959ff89ed3b403badeb77d74f1b5da8 |
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| Source note | uspto-grants-2011_09 |
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