HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 75157Erstellt: 23. Oktober 2026
Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → HCID 59437175, Verbindung
https://huagongshe.com/de/reaction/75157
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tricyclo(3.3.1.13,7)dec-1-ylmethylamine | HCID 86625 | — |
| Edukt | (S)-tert-butyl 2-(t-butyldimethylsilyloxymethyl)aziridine-1-carboxylate | HCID 72525716 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 59437175 | HCID 59437175 | 42,5% |
Reaktionsschritte
To a solution of (1-adamantylmethyl)amine (15 g, 52 mmol) in anhydrous CH2Cl2 (50 mL) was added tert-butyl 2-((tert-butyldimethylsilyloxy)methyl)aziridine-1-carboxylate (13 g, 78.3 mmol). The mixture was stirred for 10 min, the solvent was removed in vacuo and the residue was stirred at 40° C. for 5 h. The mixture was diluted with EtOAc (500 mL) and washed with water (100 mL),1N aq HCl (50 mL), satd aq NaHCO3 (50 ml) and brine (50 mL), and dried over MgSO4. The solution was concentrated to give a residue, which was purified by chromatography on silica gel to give (S)-tert-butyl 1-(tert-butyldimethylsilyloxy)-3-((1-adamantylmethyl)amino)propan-2-ylcarbamate (10 g, 24%). 1H NMR: (CDCl3, 400 MHz): δ=0.041 (s, 6H), 0.882 (s, 9H), 1.44 (s, 9H), 1.49 (s, 6H), 1.65 (m, 6H), 1.94 (s, 3H), 2.23 (s, 2H), 2.62-2.81 (m, 2H), 3.67 (m, 3H), 5.30 (s, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08835426B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-b12f6b0d30474bdbb69a09795a73ce18 |
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| Quellennotiz | uspto-grants-2014_09 |
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