HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 515729Erstellt: 25. Oktober 2026
Hydrochloric Acid → 7-Methoxy-8-methyl-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-one
https://huagongshe.com/reaction/515729
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Methyl Acrylate | HCID 7294 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | ethyl 5-methoxy-4-methyl-1H-indole-2-carboxylate | HCID 21396313 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 7-Methoxy-8-methyl-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-one | HCID 67249703 | — |
Reaktionsschritte
To a suspension of ethyl 5-methoxy-4-methyl-1H-indole-2-carboxylate (712 mg, 3.05 mmol) in toluene (10 mL) was added a 1 M solution of KOtBu in THF (3.97 mL, 3.97 mmol). The reaction mixture was stirred at room temperature for 5 min, methyl acrylate (825 μL, 9.15 mmol) was added. The reaction was stirred at reflux overnight and neutralized with 1 N HCl aqueous solution. The solid was collected and divided into three microwave vial. Each was added AcOH (8 mL) and H2O (1 mL), and heated at 180° C. for 15 min under microwave irradiation. The solvent was evaporated and the residue was purified by silica gel column chromatography to give the title compound as a yellow solid (500 mg). LCMS m/z=216.2 [M+H]+; 1H NMR (400 MHz, CDCl3) δ ppm 2.45 (s, 3H), 3.21 (t, J=6.5 Hz, 2H), 3.68 (s, 3H), 4.40 (t, J=6.2 Hz, 2H), 6.98 (s, 1H), 7.13 (d, J=9.0 Hz, 1H), 7.23 (d, J=9.0 Hz, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09108969B2 |
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| Quelldatensatz | uspto-grants-2015_08 |
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| ORD ID | ord-9662b9e604d14456a6dddab211201da2 |
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| Quellennotiz | uspto-grants-2015_08 |
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