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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 850142Erstellt: 24. Oktober 2026

Tyrosine Methyl Ester → O-(tert-butyldiphenylsilyl)-L-tyrosine methyl ester

https://huagongshe.com/de/reaction/850142

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTyrosine Methyl EsterHCID 70652—
EduktDiisopropylethylamineHCID 81531—
Edukttert-ButyldiphenylchlorosilaneHCID 94078—
LösungsmittelDichloromethaneHCID 6344—
ProduktO-(tert-butyldiphenylsilyl)-L-tyrosine methyl esterHCID 5390550587,8%

Reaktionsschritte

To a solution of L-tyrosine methyl ester (Sigma Chemical Company) (10.0 g, 51.3 mmol) and diisopropylethylamine (25.9 g, 200.0 mmol) in CH2Cl2 (400 mL) was added t-butyldiphenylsilyl chloride (TBDPS-Cl; 35.2 g, 128.2 mmol) at 23° C. The resultant mixture was stirred at 23° C. for 14 hours. The crude reaction mixture was dried over (MgSO4) and concentrated in vacuo. The resultant residue was purified by silica gel flash column chromatography. The polarity of the eluting solvent mixture was adjusted according to the Rf value of the product. The eluted fractions were combined, dried over MgSO4, concentrated and dried to give 19.5 g (87.8% yield) of O-(tert-butyldiphenylsilyl)-L-tyrosine methyl ester as a colorless syrup. Rf (hexanes/ethyl acetate (AcOEt)/methanol (MeOH) 20:20:1)=0.38.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06015887
Quelldatensatzuspto-grants-2000_01
ORD IDord-87039577dfd94d8998a5be8198a65934
Quellennotizuspto-grants-2000_01