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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1662572Generated: October 26, 2026

Tetrahydrofuran → (4R)-3-((3R)-3-(3-Isoxazolyl)-3-(3-((phenylmethyl)oxy)phenyl)propanoyl)-4-(phenylmethyl)-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/1662572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBromoetheneHCID 11641—
ReactantDi-tert-butyl dicarbonateHCID 90495—
Reactant(4R)-3-((3R)-4-Nitro-3-(3-((phenylmethyl)oxy)phenyl)butanoyl)-4-(phenylmethyl)-1,3-oxazolidin-2-oneHCID 57706543—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
Product(4R)-3-((3R)-3-(3-Isoxazolyl)-3-(3-((phenylmethyl)oxy)phenyl)propanoyl)-4-(phenylmethyl)-1,3-oxazolidin-2-oneHCID 5770675875.6%

Reaction Steps

At room temperature, di-t-butyl dicarbonate (0.502 g, 2.30 mmol) was added to a solution of (R)-4-benzyl-3-((R)-3-(3-(benzyloxy)phenyl)-4-nitrobutanoyl)oxazolidin-2-one (94.1B) (0.727 g, 1.53 mmol), vinyl bromide, (1.0 M solution in THF (16.9 mL, 16.9 mmol), N,N-dimethylpyridin-4-amine (DMAP) (0.0187 g, 0.153 mmol) and TEA (0.256 mL, 1.84 mmol). The mixture was stirred at room temperature for 24 hours. The reaction was then diluted with EtOAc (200 mL) and washed with sodium bicarbonate solution and brine. The organic phase was dried over anhydrous sodium sulfate. After removing solvent, the residue was purified by flash chromatography (silica gel, 1:2 EtOAc/hexane) and gave 558 mg of 94.1C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030354B2
Source datasetuspto-grants-2011_10
ORD IDord-0062dd5d02c74e3c9977ec5de3a01767
Source noteuspto-grants-2011_10