Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 370849Erstellt: 25. Oktober 2026

Diethyl Ether → HCID 18598657, Verbindung

https://huagongshe.com/reaction/370849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktDI-Tert-butyl bromomalonateHCID 11392273—
Edukttert-Butyl L-alanyl-L-prolinateHCID 12939800—
LösungsmittelTolueneHCID 1140—
ProduktHCID 18598657HCID 18598657—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Di-t-butyl bromomalonate (15.9 g.) was added to a stirred solution of L-alanyl-L-proline t-butyl ester (26 g.) in toluene (30 ml.) which was cooled to 0° C., and the mixture was allowed to warm up to laboratory temperature during 2 hours and was stirred at that temperature for 14 hours. Diethyl ether (300 ml.) was added, the mixture was filtered to remove unreacted L-alanyl-L-proline t-butyl ester as the hydrobromide salt thereof, andthe filtrate was evaporated to dryness under reduced pressure. The residue was dissolved in ethyl acetate (400 ml.) and the mixture was washed successively twice with aqueous 0.5N-citric acid solution (100 ml. each time), once with water (100 ml.) and once with saturated aqueous sodium chloride solution (100 ml.), dried over magnesium sulphate and evaporated to dryness under reduced pressure. The residue was purified by chromatography on a silica gel column using a 9:1 v/v mixture of dichloromethane and ethyl acetate as eluant, and there was thus obtained as an oil N-[di-t-butoxycarbonylmethyl]-L-alanyl-L-proline t-butyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04528282
Quelldatensatzuspto-grants-1985_07
ORD IDord-ea688f8b6eb5482f8421f825ed0ed365
Quellennotizuspto-grants-1985_07