HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 571195Erstellt: 26. Oktober 2026
Potassium Carbonate → methyl 2-(7-nitro-1H-indol-1-yl)acetate
https://huagongshe.com/reaction/571195
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 7-Nitroindole | HCID 23396 | — |
| Edukt | Methyl bromoacetate | HCID 60984 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | methyl 2-(7-nitro-1H-indol-1-yl)acetate | HCID 86681614 | 51% |
Reaktionsschritte
To a solution of 7-nitro-1H-indole (0.5 g, 3.08 mmol) in dry CH3CN (20 ml), K2CO3 (0.511 g, 3.70 mmol) was added at room temperature. After 10 minutes, methyl 2-bromoacetate (0.343 ml, 3.70 mmol) was added dropwise, and the reaction was refluxed for 24 hours. Additional K2CO3 (0.511 g, 3.70 mmol) and methyl 2-bromoacetate (0.343 ml, 3.70 mmol) were added, and the stirring was prolonged for further 16 hours. The reaction was cooled at room temperature and the solvent was evaporated under vacuum. The resulting crude was partitioned between water and DCM; the organic phase was dried over sodium sulfate and evaporated under vacuum. The crude was purified by flash column chromatography on silica gel (hexane:ethyl acetate=9:1) affording methyl 2-(7-nitro-1H-indol-1-yl)acetate that crystallizes on standing (0.37 g, 1.580 mmol, 51% yield). MS/ESI+ 234.9 [MH]+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09024027B2 |
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| Quelldatensatz | uspto-grants-2015_05 |
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| ORD ID | ord-3b88eb2600b1460fb4224f3d9fb5ecd4 |
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| Quellennotiz | uspto-grants-2015_05 |
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