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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 358301Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/358301

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
PatentnummerUS04465844
Quelldatensatzuspto-grants-1984_08
ORD IDord-7f80ed19ce8148eea873befe7a1827be
Quellennotizuspto-grants-1984_08