HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11486Erstellt: 24. Oktober 2026
Methanol → 2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl) ethyl]-N-pentylamide
https://huagongshe.com/de/reaction/11486
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methanol | HCID 887 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Oxydiacetyl dichloride | HCID 88769 | — |
| Edukt | 2-(1Adamantyl)-n-pentylethylamine hydrochloride | HCID 49831680 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl) ethyl]-N-pentylamide | HCID 57481273 | 60% |
Reaktionsschritte
2-(1-Adamantyl)-N-pentylethylamine hydrochloride (Intermediate No. 1-1) (0.50 g, 1.7 mmol) was added to a solution of diglycolyl chloride (0.31 ml, 2.6 mmol) and triethylamine (0.70 ml, 5.1 mmol) in anhydrous dichloromethane (6 ml) under ice-cooling, and the mixture was stirred at room temperature overnight. Methanol (5 ml) was added to the reaction mixture, and the whole was stirred for three hours. The solvent was evaporated under reduced pressure, the residue was distributed with ethyl acetate and water (15 ml respectively), and the organic layer was washed with a saturated aqueous sodium chloride solution (5 ml) and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, the resulting residue was purified by silica gel column chromatography to give 0.39 g (60%) of 2-methoxycarbonylmethoxyacetic acid N-[2-(1-adamantyl)ethyl]-N-pentylamide as an oily matter.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07098226B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-255a07025eca44d1b3ec05d62aa736eb |
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| Quellennotiz | uspto-grants-2006_08 |
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