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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 416348Erstellt: 24. Oktober 2026

Formaldehyde → (S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylate

https://huagongshe.com/de/reaction/416348

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
Eduktp-Toluenesulfonic acidHCID 6101—
EduktN-CarbethoxyphthalimideHCID 31187—
EduktN-alpha-Benzyloxycarbonyl-L-ornithineHCID 7010490—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt(S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylateHCID 5438015676%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

A mixture of (S)-5-amino-2-(benzyloxycarbonylamino)pentanoic acid (10.0 g, 37.56 mmol), ethyl 1,3-dioxoisoindoline-2-carboxylate (9.04 g, 41.28 mmol) in NMP (40.0 mL) was heated to 150° C. for 30 min in 4 microwave reaction tubes. The mixture was diluted with EtOAc (500 mL). The organic layer washed with water (100 mL×2), brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give an oil, which was dissolved in toluene. To this toluene solution was added paraformaldehyde, PTSA and molecular sieves (3 Å) and the mixture was heated to 150° C. for 20 min. The mixture was diluted with ether (800 mL), washed with NaHCO3, brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-benzyl 4-(3-(1,3-dioxoisoindolin-2-yl)propyl)-5-oxooxazolidine-3-carboxylate (11.6 g, 76% for 2 steps).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08088793B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-72832e885ee74b96ab642b978891e8de
Quellennotizuspto-grants-2012_01