HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 242659Erstellt: 26. Oktober 2026
Acetaldehyde → Tert-butyl 3-(ethylamino)pyrrolidine-1-carboxylate
https://huagongshe.com/reaction/242659
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetaldehyde | HCID 177 | — |
| Edukt | (R)-(+)-1-Boc-3-aminopyrrolidine | HCID 854070 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Tert-butyl 3-(ethylamino)pyrrolidine-1-carboxylate | HCID 20800658 | — |
Reaktionsschritte
To a solution of (R)-3-amino-1-N-Boc pyrrolidine (1 eq, 5.37 mmol) in methanol (20 mL) was added acetaldehyde (0.95 eq) and the resulting mixture was heated to 80° C. and stirred for 2 h., then stirred at room temperature overnight. Sodium borohydride (0.95 eq, 5.1 mmol) was added and reaction mixture was stirred for an additional 2 h. The reaction mixture was concentrated, dissolved in ethyl acetate and washed with saturated aqueous sodium bicarbonate. The combined organics were washed with brine and dried over sodium sulfate. The crude product was purified on silica using hexane/ethyl acetate (10%) to hexane/ethyl acetate (50%). 1H-NMR (CDCL3) δ: 1.05 (3H, t), 1.45 (9H, s), 1.60-1.75 (1H, m), 2.00-2.10 (1H, m), 2.68 (4H, q), 2.90-3.15 (1H, m), 3.25-3.65 (4H, m). ESI-MS m/z: 215 (M+1), UV retention time: 0.75 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08653096B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-6de36c0f01444b1d873210d6f2fcf513 |
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| Quellennotiz | uspto-grants-2014_02 |
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