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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 18046Erstellt: 26. Oktober 2026

Tetrahydrofuran → Carbamate

https://huagongshe.com/reaction/18046

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktBenzyl chloroformateHCID 10387—
EduktSodium BicarbonateHCID 516892—
EduktL-Tyrosine 1,1-dimethylethyl esterHCID 6950582—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
ProduktCarbamateHCID 276—
ProduktZ-Tyr-OtBuHCID 11428694—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a 0° C. suspension of L-tyrosine tert-butyl ester (Bachem, 1.0. eq) and sodium bicarbonate (2.0 eq) in a 1:1 mixture of THF and water was added slowly with stirring benzyl chloroformate (1. 1 eq). After the addition, the mixture was stirred at 0° C. for 3 h and at room temperature for 24 h. The mixture was diluted with diethyl ether, and the aqueous layer was separated. The organic extracts were washed with saturated sodium chloride, treated with anhydrous magnesium sulfate, filtered, and evaporated to afford N-benzyloxycarbonyl-L-tyrosine tert-butyl ester of sufficient purity for immediate conversion of the tyrosine hydroxyl into a carbamate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07741328B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-4a6c1f1dc3e74d41b45ee6e37120b17a
Quellennotizuspto-grants-2010_06