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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 891667Erstellt: 24. Oktober 2026

Hexane → N-((Phenylmethoxy)carbonyl)-L-serine methyl ester

https://huagongshe.com/de/reaction/891667

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
EduktN-(Benzyloxycarbonyl)-L-serineHCID 100310—
EduktTrimethylsilyldiazomethaneHCID 167693—
LösungsmittelBenzeneHCID 241—
LösungsmittelMethanolHCID 887—
ProduktN-((Phenylmethoxy)carbonyl)-L-serine methyl esterHCID 6999535100%

Reaktionsschritte

To a solution of N-carbobenzyloxy-L-serine (4.0 g, 16.7 mmol) in benzene (200 ml) and methanol (50 ml) was added a solution of 2M trimethylsilyldiazomethane in hexane (10.9 ml, 21.7 mmol) in an ice bath, and the mixture was stirred at room temperature for 3 hours. After checking the completion of the reaction, the reaction mixture was concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using n-hexane:ethyl acetate (1:1→1:3) as the eluant to afford N-carbobenzyloxy-L-serine methyl ester (4.40 g, yield 100%) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07001897B2
Quelldatensatzuspto-grants-2006_02
ORD IDord-4b434369fbc940f9a0701f5badd41222
Quellennotizuspto-grants-2006_02