HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 520352Erstellt: 25. Oktober 2026
Di-tert-butyl dicarbonate → HCID 10331393, Verbindung
https://huagongshe.com/reaction/520352
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Edukt | (S)-3-Azido-4,4-dimethyldihydrofuran-2(3H)-one | HCID 10057735 | — |
| Katalysator | Palladium | HCID 23938 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | HCID 10331393 | HCID 10331393 | — |
Reaktionsschritte
To a solution of (S)-3-azido-4,4-dimethyldihydrofuran-2(3H)-one (5.52 g) in MeOH 910 mL) was added 10% Pd/C (0.379 g, 0.356 mmol) under N2. The reaction mixture was stirred under H2 at rt for 16 hrs. The reaction was filtered through diatomaceous earth (Celite®), washed with EtOAc and the filtrate was concentrated to yield a clear oil. To the above oil in DCM (10 mL) was added BOC2O (9.09 mL) and TEA (13.88 mL). The reaction mixture was stirred at rt for 16 hrs. The reaction mixture was diluted with EtOAc, washed with sat. NaHCO3, citric acid, water, sat. NaCl, dried over anhydrous Na2SO4, filtered and concentrated to yield an oil. The crude product was purified by silica gel chromatography (0-100% EtOAc in hexane) to yield (S)-tert-butyl 4,4-dimethyl-2-oxotetrahydrofuran-3-ylcarbamate (3.8 g) as a white solid. LC/MS (Cond. N-1): [M+Na]+ 252.06, RT=2.75 min. 1H NMR (400 MHz, CHLOROFORM-d) ppm 4.81-4.95 (1H, m), 4.38 (1H, d, J=7.78 Hz), 3.97-4.07 (2H, m), 1.47 (9H, s), 1.25 (3H, s), 1.01 (3H, s).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09326973B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-2500128def064324a78f9ab3b52dfdd6 |
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| Quellennotiz | uspto-grants-2016_05 |
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