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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27347Erstellt: 24. Oktober 2026

4-Methylmorpholine → carbobenzoxy-beta-alanyl-L-proline t-butyl ester

https://huagongshe.com/de/reaction/27347

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktIsobutyl chloroformateHCID 62365—
EduktN-Benzyloxycarbonyl-beta-alanineHCID 75313—
Edukttert-Butyl L-prolinate hydrochlorideHCID 6453107—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelTriethylamineHCID 8471—
Produktcarbobenzoxy-beta-alanyl-L-proline t-butyl esterHCID 54135485—

Reaktionsschritte

4.46 g. of carbobenzoxy-β-alanine is dissolved in 20 ml. of tetrahydrofuran and the resulting solution cooled to -10° C. With constant stirring of the solution, 2.4 ml. of N-methylmorpholine followed by 2.6 ml. of isobutylchloroformate are added and the resulting reaction mixture is stirred thereafter for approximately 5 minutes at -10° C. 4.16 g. of L-proline t-butyl ester hydrochloride in 20 ml. of dimethylformamide and 2.8 ml. of triethylamine is added to the reaction mixture which is thereafter stirred overnight, while slowly warming to room temperature. The solvent of the reaction mixture is evaporated in vacuo at 30°-35°. The residue is dissolved in 800 ml. of ethyl acetate which is washed with (2×150 ml.) a 10% citric acid solution, with (1×150 ml.) water, with (2×150 ml.) saturated solution of sodium bicarbonate and then with (2×100 ml.) water. The organic layer is dried with anhydrous magnesium sulfate and the solvent evaporated to yield carbobenzoxy-β-alanyl-L-proline t-butyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04221706
Quelldatensatzuspto-grants-1980_09
ORD IDord-c7cd6af73aca49feafad7a587907044d
Quellennotizuspto-grants-1980_09