HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 860708Erstellt: 24. Oktober 2026
Sodium hydride → Methyl 3-cyclohexyl-1-(2-(methoxycarbonyl)allyl)-2-(2-vinylphenyl)-1H-indole-6-carboxylate
https://huagongshe.com/de/reaction/860708
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2-Propenoic acid, 2-(bromomethyl)-, methyl ester | HCID 521093 | — |
| Edukt | methyl 3-cyclohexyl-2-(2-vinylphenyl)1H-indole-6-carboxylate | HCID 58765232 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Methyl 3-cyclohexyl-1-(2-(methoxycarbonyl)allyl)-2-(2-vinylphenyl)-1H-indole-6-carboxylate | HCID 58765271 | 100,1% |
Reaktionsschritte
Methyl 3-cyclohexyl-2-(2-vinylphenyl)-1H-indole-6-carboxylate (7, R2=H) 508 mg, 1.4 mmol) was dissolved in THF (5 mL) under N2 and cooled to 0° C. Sodium hydride (143 mg, 60% suspension in mineral oil, 3.57 mmol) was added and the mixture was stirred at 0° C. for 5 min, when a solution of methyl 2-(bromomethyl)acrylate (276 mg, 1.54 mmol) in THF (1.5 mL) was added dropwise. Stirring was continued for 30 min at 22° C. The reaction was quenched with a saturated aqueous solution of ammonium chloride (20 mL) and extracted with EtOAc (2×30 mL) and CH2Cl2 (30 mL). The organic extracts were combined and dried over sodium sulfate, filtered and concentrated. The residue was chromatographed on silica gel using hexane/ethyl acetate (0–20%) to afford the title compound as a pale yellow solid (641 mg, 99%). ESI-MS m/z 458 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07153848B2 |
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| Quelldatensatz | uspto-grants-2006_12 |
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| ORD ID | ord-2337b15bed044708801a2995f2b94e49 |
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| Quellennotiz | uspto-grants-2006_12 |
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