Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426092Generated: November 1, 2026

Tetrahydrofuran → Carbamate

https://huagongshe.com/reaction/2426092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
ReactantL-Tyrosine 1,1-dimethylethyl esterHCID 6950582—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductCarbamateHCID 276—
ProductZ-Tyr-OtBuHCID 11428694—

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968547B2
Source datasetuspto-grants-2011_06
ORD IDord-c5fd009872d44c28bf1fca73d5015d57
Source noteuspto-grants-2011_06