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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 34529Erstellt: 23. Oktober 2026

Dicyclohexylcarbodiimide → Benzyl N-(2-oxopentanoyl)prolinate

https://huagongshe.com/de/reaction/34529

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt2-Oxovaleric acidHCID 74563—
EduktDiisopropylethylamineHCID 81531—
EduktProline benzyl ester hydrochlorideHCID 2733413—
LösungsmittelDichloromethaneHCID 6344—
ProduktBenzyl N-(2-oxopentanoyl)prolinateHCID 53809756—

Reaktionsschritte

8.8 g benzyl prolinate hydrochloride, 9.78 g dicyclohexylcarbodiimide and 6.12 g diisopropylethylamine were reacted together in 50 mL dichloromethane at 0°. 5.51 g 2-oxopentanoic acid in 10 mL dichloromethane was added dropwise at 0°. The pH of the reaction was adjusted to between 8 and 9 with diisopropylethylamine. The reaction mixture was stirred for four hours at 0°, then room temperature overnight. The next day, the reaction mixture was filtered, concentrated to dryness, and partitioned between ethyl acetate and water. The organic layer was washed with 5% sodium bisulfate, 5% sodium bicarbonate, and saturated sodium chloride solutions, and dried with magnesium sulfate. The organic layer was concentrated to give a yellow oil. The oil was then passed through a silica gel column and eluted with ethyl acetate/hexane (4:6) and ethyl acetate/hexane (1:1). Benzyl N-(2-oxopentanoyl)prolinate, [α]D25 -56.9, was isolated.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04762821
Quelldatensatzuspto-grants-1988_08
ORD IDord-1518e2ac8a1d43678cc8596fcb89ca73
Quellennotizuspto-grants-1988_08