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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1903602Erstellt: 26. Oktober 2026

Triphenylphosphine → Benzyloxycarbonyl-2-[1-(2,4-dimethoxybenzyl)-2,5-dioxopyrrolidin-3-yl] glycine methyl ester

https://huagongshe.com/reaction/1903602

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt2,4-Dimethoxybenzyl alcoholHCID 81750—
Eduktethyl N-ethoxycarbonyliminocarbamateHCID 220568—
EduktBenzyloxycarbonyl-2-(2,5-dioxopyrrolidin-3-yl)glycine methyl esterHCID 13105389—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBenzyloxycarbonyl-2-[1-(2,4-dimethoxybenzyl)-2,5-dioxopyrrolidin-3-yl] glycine methyl esterHCID 20449787—

Reaktionsschritte

In 100 ml of tetrahydrofuran were dissolved 3.2 g of benzyloxycarbonyl-2-(2,5-dioxopyrrolidin-3-yl)glycine methyl ester, 1.8 g of 2,4-dimethoxybenzyl alcohol and 3.9 g of triphenylphosphine and under ice-cooling 2 ml of diethyl azodicarboxylate was added. The mixture was stirred at room temperature for one hour and concentrated under reduced pressure. The residue was dissolved in ethyl acetate, and the solution was washed with 5% sodium hydrogen carbonate and 10% phosphoric acid in that order and dried over sodium sulfate. The solution was concentrated under reduced pressure and the concentrate was chromatographed on a silica gel column, elution being carried out with toluene-ethyl acetate (7:3). The eluate was concentrated under reduced pressure and to the residue was added petroleum ether. The precipitate was collected by filtration and dried. Yield 1.2 g

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04436918
Quelldatensatzuspto-grants-1984_03
ORD IDord-7a45b318a5c649daa32cb85a0cceafb2
Quellennotizuspto-grants-1984_03