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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297573Generated: October 29, 2026

Tetrahydrofuran → Carbamate

https://huagongshe.com/reaction/2297573

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 numberUS06492372B1
Source datasetuspto-grants-2002_12
ORD IDord-2d129c3a9424412c93a8ed9c81d47739
Source noteuspto-grants-2002_12