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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 369799Erstellt: 25. Oktober 2026

tert-butyl (2R,3S)-6-oxo-2,3-diphenylmorpholine-4-carboxylate → HCID 57135938, Verbindung

https://huagongshe.com/reaction/369799

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-butyl (2R,3S)-6-oxo-2,3-diphenylmorpholine-4-carboxylateHCID 981230—
EduktSodium bis(trimethylsilyl)amideHCID 2724254—
Edukt3-Cyclobutylbenzyl bromideHCID 18352491—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 57135938HCID 5713593854,1%

Reaktionsschritte

According to example 81, 2.50 g of tert-butyl- (2R, 3S)-(-)-6-oxo-2,3-diphenyl-4-morpholinecarboxylate (Aldrich) was alkylated with 1.59 g of 3-cyclobutylbenzyl bromide in 80 mL of anhydrous THF using 7.41 mL of 1M sodium bis(trimethylsilyl)amide in THF (Aldrich). The crude product was subjected to flash chromatography on 120 g of silica gel (8:2 hexane:EtOAc) and then recrystallization from EtOH-water to afford 1.90 g (54%) of tert-butyl (2R, 3S, 5S)-6-oxo-2,3-diphenyl-5-(3-cyclobutylbenzyl)-4-morpholinecarboxylate as a white powder, m.p. 145-147° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06140100
Quelldatensatzuspto-grants-2000_10
ORD IDord-a0731c46a2c343749606ce782d6325e2
Quellennotizuspto-grants-2000_10