HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 41063Erstellt: 26. Oktober 2026
Potassium Carbonate → 5-Cyclopropylmethoxy-1H-indol
https://huagongshe.com/reaction/41063
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 5-Hydroxyindole | HCID 16054 | — |
| Edukt | Bromomethylcyclopropane | HCID 81503 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | 5-Cyclopropylmethoxy-1H-indol | HCID 57436983 | — |
Reaktionsschritte
To a solution of 7.3 g 5-hydroxy-indole in 130 ml of dry acetone are added 10.5 ml bromomethyl cyclopropane and 22.7 g anhydrous potassium carbonate. The mixture is heated to reflux for 24 h and an additional amount of 5 ml bromomethyl cyclopropane are added. The mixture is heated to reflux for additional 4 days. The mixture is filtered and the solvent is removed under reduced pressure. The residue is dissolved in dichloro methane and washed with an aqueous solution of hydrochloric acid (2 M), 10% aq. NaHCO3 and water. The organic layer is dried and the solvent is removed under reduced pressure. After purification by column chromatography (silica gel; toluene, acetone 95:5), 9.62 g, 94%) of the title compound are obtained as an oil. 1H-NMR (CDCl3): 0.36 (m, 2H, cyclopropyl CH2), 0.64 (m, 2H, cyclopropyl CH2), 1.30 (m, 1H, cyclopropyl CH), 3.83 (d, 2H, J=7.0 Hz, CH2O), 6.45 (s, 1H, aromatic), 6.90 (dd, 1H, aromatic), 7.09-7.27 (m, 3H, aromatic), 8.05 (bs, 1H, NH). 13C-NMR (CDCl3): 3.1 (2 cyclopropyl CH2), 10.4 (cyclopropyl CH), 74.2 (CH2O), 101.2, 101.6, 104.0, 104.6, 149.8 (aromatic)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08530493B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-6920e4434f3d4db69bd1d676b22b48e8 |
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| Quellennotiz | uspto-grants-2013_09 |
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