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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1721716Generated: October 30, 2026

Ethyl Acetate → methanesulphonic acid (4S,5S)-4-benzyl-2-oxo-oxazolidin-5-ylmethyl ester

https://huagongshe.com/reaction/1721716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant(4S,5S)-5-hydroxymethyl-4-phenylmethyloxazolidinoneHCID 9859125—
SolventAcetoneHCID 180—
Solvent4-MethylmorpholineHCID 7972—
Productmethanesulphonic acid (4S,5S)-4-benzyl-2-oxo-oxazolidin-5-ylmethyl esterHCID 57150902100%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 4.7 ml of methanesulphonyl chloride in 10 ml of acetone is added at 25° C. to a suspension of 10.4 g of the alcohol from Example 8 in 20 ml of acetone and 6.1 ml of N-methylmorpholine and the suspension is stirred at 25° C. for 3 hours. A further 1.1 ml of N-methylmorpholine are added and the mixture is stirred for 1 hour. The suspension is shaken with 80 ml of semi-saturated NaHCO3 solution and ethyl acetate and the separated aqueous phase is extracted with ethyl acetate. The ethyl acetate extracts are washed with water, dried and filtered. The filtrate is concentrated to give 14.3 g (100%) of crude methanesulphonic acid (4S,5S)-4-benzyl-2-oxo-oxazolidin-5-ylmethyl ester, TLC (SiO2 ethyl acetate): Rf =0.4; MS (EI): 286 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05512688
Source datasetuspto-grants-1996_04
ORD IDord-db03d090bde1488fabd36d012943c37d
Source noteuspto-grants-1996_04