Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 493081Erstellt: 26. Oktober 2026

2(3H)-Benzoxazolone → 3-(3-amino-3-methyl-butyl)-3H-benzoxazol-2-one

https://huagongshe.com/reaction/493081

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2(3H)-BenzoxazoloneHCID 6043—
EduktSodium hydrideHCID 24758—
EduktSodium BicarbonateHCID 516892—
Edukttert-butyl N-(4-amino-2-methylbutan-2-yl)carbamateHCID 45072487—
EduktTert-butyl [1,1-dimethyl-3-(2-oxobenzooxazol-3-yl)propyl]carbamateHCID 57435843—
KatalysatorTetrabutylammonium IodideHCID 67553—
LösungsmittelEthyl AcetateHCID 8857—
Lösungsmittel2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
Produkt3-(3-amino-3-methyl-butyl)-3H-benzoxazol-2-oneHCID 57435838—

Reaktionsschritte

tert-butyl[1,1-dimethyl-3-(2-oxo-benzoxazol-3-yl)-propyl]-carbamate: 4.0 g (29.6 mmol) benzoxazol-2-one are dissolved in 40 mL DMPU and cooled with an ice bath. Under protective gas 897 mg (95%; 35.5 mmol) sodium hydride is added batchwise to this solution. The reaction mixture is heated to ambient temperature and then stirred for another hour. 9.85 g (44.4 mmol) tert-butyl (3-amino-1,1-dimethyl-propyl)-carbamate and 1.97 g (5.3 mmol) tetrabutylammonium iodide are added and the mixture is stirred overnight. The reaction is stopped by the careful addition of sodium hydrogen carbonate solution. Ethyl acetate is added, the aqueous phase is separated off and extracted repeatedly with ethyl acetate. The combined organic phases are washed with sodium chloride solution, dried with sodium sulphate and evaporated down. Purification of the residue by column chromatography (silica gel; petroleum ether/ethyl acetate=7:3) yields the desired product. Yield 4.1 g (43%); mass spectroscopy: [M+H]+=321.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07534789B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-829931ec9cb540ec95496c98b668fbba
Quellennotizuspto-grants-2009_05