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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369825Generated: October 27, 2026

Ethanol → 3-tert-butyl-L-tyrosine

https://huagongshe.com/reaction/369825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant(2R, 3S, 5S)-6-oxo-2,3-diphenyl-5-(3-tert-butyl-4-hydroxybenzyl)morpholineHCID 57303814—
CatalystPalladium ChlorideHCID 24290—
SolventTetrahydrofuranHCID 8028—
Product3-tert-butyl-L-tyrosineHCID 20637691105.9%

Reaction Steps

To a 300 mL Parr bottle were added 0.73 g of PdCl2 and 20 mL of 1:1 THF:EtOH. To this was added a solution of 2.43 g of (2R, 3S, 5S)-6-oxo-2,3-diphenyl-5-(3-tert-butyl-4-hydroxybenzyl)morpholine in 80 mL of 1:1 THF:EtOH. The mixture was deoxygenated by bubbling nitrogen through for 10 min and was hydrogenated at 45 psi for 18 h. The vessel was purged with nitrogen, catalyst removed by filtration, and the filtrate concentrated in vacuo. The residue was partitioned between water and hexane. The aqueous solution was washed with four additional 50 mL portions of hexane, subjected to brief rotary evaporation to remove residual hexane, frozen and lyophilized to afford 1.47 g (92%) of 3-tert-butyl-L-tyrosine.HCl as a tan hygroscopic solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140100
Source datasetuspto-grants-2000_10
ORD IDord-20643eb3f18b499ca8f371667cc9dd47
Source noteuspto-grants-2000_10