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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 520352Erstellt: 25. Oktober 2026

Di-tert-butyl dicarbonate → HCID 10331393, Verbindung

https://huagongshe.com/reaction/520352

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDi-tert-butyl dicarbonateHCID 90495—
Edukt(S)-3-Azido-4,4-dimethyldihydrofuran-2(3H)-oneHCID 10057735—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 10331393HCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09326973B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-2500128def064324a78f9ab3b52dfdd6
Quellennotizuspto-grants-2016_05