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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 274087Erstellt: 25. Oktober 2026

Pyridine → N-methoxycarbonyl-L-tyrosine benzyl ester

https://huagongshe.com/reaction/274087

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktDichloromethaneHCID 6344—
EduktMethyl chloroformateHCID 6586—
EduktO-benzyl-L-tyrosine toluene-p-sulphonateHCID 104540—
LösungsmittelWaterHCID 962—
ProduktN-methoxycarbonyl-L-tyrosine benzyl esterHCID 54118506—

Reaktionsschritte

To an ice-cooled mixture of L-tyrosine benzyl ester p-toluenesulfonate (41.0 g), pyridine (16.4 ml), and dichloromethane (92 ml) was added methyl chloroformate (7.8 ml). The mixture was stirred in an ice-bath for 1 hour, diluted with water, and extracted once with dichloromethane. The extract was concentrated in vacuo and the residue was dissolved in ethyl acetate, washed with water and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo. Purification of the crude product by column chromatography on silica gel (gradient elution; 10:1 to 5:1 chloroform-ethyl acetate) gave N-methoxycarbonyl-L-tyrosine benzyl ester (22.0 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05387710
Quelldatensatzuspto-grants-1995_02
ORD IDord-a8b25bcf9a0b44ff970acb08cc2a1871
Quellennotizuspto-grants-1995_02