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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25682Generated: October 26, 2026

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

https://huagongshe.com/reaction/25682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenylacetaldehydeHCID 13696—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactanttert-butyl (S)-(2-hydroxy-1-phenyl-ethylamino)-acetateHCID 59065869—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Producttert-butyl ((4R)-2-benzhydryl-4-phenyl-oxazolidin-3-yl)-acetateHCID 69754033114.1%

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858591B2
Source datasetuspto-grants-2005_02
ORD IDord-baf8df1b87c8452ebbf4cdc0f2992acd
Source noteuspto-grants-2005_02