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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567417Generated: October 30, 2026

Potassium Carbonate → (4S,5R)-N-(t-butylaminocarbonyl)-2-(2,4dimethoxyphenyl)-4phenyl-5-oxazolidine-carboxylic acid potassium salt

https://huagongshe.com/reaction/567417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(4S,5R)-N-(t-Butylaminocarbonyl)-2-(2,4-dimethoxyphenyl)-4-phenyl-5-oxazolidinecarboxylic acid methyl esterHCID 53753692—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product(4S,5R)-N-(t-butylaminocarbonyl)-2-(2,4dimethoxyphenyl)-4phenyl-5-oxazolidine-carboxylic acid potassium saltHCID 69748715—

Reaction Steps

(4S,5R)-N-(t-Butylaminocarbonyl)-2-(2,4dimethoxyphenyl)-4-phenyl-5-oxazolidinecarboxylic acid methyl ester (PREPARATION 2—less polar isomer, 6.27 g, 14.2 mM) is stirred at 20-25° under nitrogen in methanol (50 mL). To this mixture is added a solution of potassium carbonate (2.50 g, 18.1 mM) in water (6 mL). After 6 hr the reaction is concentrated under reduced pressure to remove the methanol and the residue freeze dried to give the title compound (admixed with potassium carbonate salts as a powder), NMR (DMSO-d6, TMS) 1.10, 3.77, 4.17, 4.70, 5.16, 6.50, 6.60 and 7.14-7.42 δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177573B1
Source datasetuspto-grants-2001_01
ORD IDord-c2eee1e4be9749f694dd41f810cc39c8
Source noteuspto-grants-2001_01