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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2117009Erstellt: 25. Oktober 2026

p-Toluenesulfonic acid → L-Tyrosine

https://huagongshe.com/reaction/2117009

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktp-Toluenesulfonic acidHCID 6101—
EduktCesium carbonateHCID 10796—
EduktMethyl bromoacetateHCID 60984—
EduktDiisopropylethylamineHCID 81531—
EduktDi-tert-butyl dicarbonateHCID 90495—
Edukt(S)-Benzyl 2-amino-3-(4-hydroxyphenyl)propanoateHCID 104541—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktL-TyrosineHCID 6057—

Reaktionsschritte

The para-toluenesulfonic acid salt of tyrosine benzyl ester (5.05 g, 11.4 mmol) was dissolved in THF (50 mL) containing DIEA (2.18 mL, 12.5 mmol) and di-tert-butyidicarbonate (2.98 g, 13.7 mmol) was added in one portion. The reaction was stirred 1.5 h at room temperature. Volatiles were removed under reduced pressure and the residue was dissolved in Et2O (150 mL). The solution was washed successively with water (25 mL), 5% citric acid (25 mL) and 5% NaHCO3 (25 mL). After drying (MgSO4), the solvent was evaporated under reduced pressure and the residue dissolved in acetone (100 mL). Cesium carbonate (4.83 g, 14.8 mmol) and methyl bromoacetate (1.3 mL, 13.7 mmol) were added and the heterogeneous mixture was stirred overnight at room temperature. Solids were then removed by filtration (acetone for washings) and the filtrate evaporated. The residue was dissolved in Et2O (150 mL) and washed with water (25 mL) and brine (25 mL). After drying (MgSO4), the solution was concentrated and the residue purified by flash chromatography using 25-50% EtOAc/hexane as eluent. The fully protected tyrosine derivative was obtained as a colorless oil (3.61 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07439258B2
Quelldatensatzuspto-grants-2008_10
ORD IDord-18db573d8e324bb38d3060ded58b676d
Quellennotizuspto-grants-2008_10