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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25682Erstellt: 23. Oktober 2026

Diphenylacetaldehyde → tert-butyl ((4R)-2-benzhydryl-4-phenyl-oxazolidin-3-yl)-acetate

https://huagongshe.com/de/reaction/25682

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiphenylacetaldehydeHCID 13696—
EduktSulfuric acid magnesium salt (1:1)HCID 24083—
Edukttert-butyl (S)-(2-hydroxy-1-phenyl-ethylamino)-acetateHCID 59065869—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-butyl ((4R)-2-benzhydryl-4-phenyl-oxazolidin-3-yl)-acetateHCID 69754033114,1%

Reaktionsschritte

To a solution of tert-butyl (S)-(2-hydroxy-1-phenyl-ethylamino)-acetate (2.5 g, 10 mmole, obtained from Reference Example 9) in anhydrous methylene chloride (35 ml) were added diphenylacetaldehyde (2.16 g, 11 mmole) and magnesium sulfate (1.2 g, 10 mmole) under nitrogen. The resulting mixture was stirred at room temperature under nitrogen for 15 h, and diluted with ether. The organic layer was washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered and concentrated to dryness in vacuo. The oily residue was solidified upon standing, and recrystallized from ether/hexanes to give tert-butyl ((4R)-2-benzhydryl-4-phenyl-oxazolidin-3-yl)-acetate as a white solid (4.9 g, 98%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858591B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-baf8df1b87c8452ebbf4cdc0f2992acd
Quellennotizuspto-grants-2005_02