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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739447Generated: October 31, 2026

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

https://huagongshe.com/reaction/1739447

Reaction equation

Participants

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

Reaction Steps

A 100 mg (0.23 mM) quantity the less polar isomer of (4S,5R)-N-(t-butylamino-carbonyl)-2-(2,4-dimethoxyphenyl)-4phenyl-5-oxazolidinecarboxylic acid methyl ester (Preparation 57, 5Ka) is stirred at room temperature under nitrogen in 3 mL MeOH. To this is added 0.1 mL water and 43 mg (0.31 mM) potassium carbonate. After 1 hour, TLC shows no starting material left. Store in freezer overnight. The next morning the solvent is evaporated to give (4S,5R)-N-(t-butylaminocarbonyl)-2-(2,4dimethoxyphenyl)-4phenyl-5-oxazolidine-carboxylic acid potassium salt (6Ka).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965739
Source datasetuspto-grants-1999_10
ORD IDord-66ef6e00ead448cfadfe38113ff977e7
Source noteuspto-grants-1999_10