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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1418787Erstellt: 26. Oktober 2026

Sodium hydride → N-benzyloxycarbonyl-3-[4-(1,4,7-trioxaoctyl)-phenyl]-alanine-methyl ester

https://huagongshe.com/reaction/1418787

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt1-Bromo-3,6-dioxaheptaneHCID 123532—
EduktSodium BicarbonateHCID 516892—
EduktN-[(Phenylmethoxy)carbonyl]-L-tyrosine methyl esterHCID 7010613—
LösungsmittelTolueneHCID 1140—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-benzyloxycarbonyl-3-[4-(1,4,7-trioxaoctyl)-phenyl]-alanine-methyl esterHCID 22940770—

Reaktionsschritte

6.59 g (20 mmol) of N-benzyloxycarbonyl-tyrosine-methyl ester is dissolved in 25 ml of anhydrous N,N-dimethylformamide and mixed at 0° C. under argon with 0.81 g (20.5 mmol) of sodium hydride dispersion (60% in mineral oil). The batch is allowed to stir for 10 minutes, then 3.75 g (20.5 mmol) of 1-bromo-2-(2-methoxyethoxy)-ethane is added, the reaction temperature is allowed to increase to room temperature and stirred for another three hours. For working-up, the batch is taken up in toluene and shaken out several times against aqueous sodium bicarbonate solution. The organic phase is separated, dried on magnesium sulfate, filtered and concentrated by evaporation. The oily residue is chromatographed for purification on silica gel with hexane/diethyl ether/triethylamine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05885548
Quelldatensatzuspto-grants-1999_03
ORD IDord-1341ac2f27f648288d7130e58f5f5e93
Quellennotizuspto-grants-1999_03