HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209749Generated: October 29, 2026
Ethyl Acetate → methanesulphonic acid (4S,5S)-4-benzyl-2-oxo-oxazolidin-5-ylmethyl ester
https://huagongshe.com/reaction/2209749
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (4S,5S)-5-hydroxymethyl-4-phenylmethyloxazolidinone | HCID 9859125 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | 4-Methylmorpholine | HCID 7972 | — |
| Product | methanesulphonic acid (4S,5S)-4-benzyl-2-oxo-oxazolidin-5-ylmethyl ester | HCID 57150902 | 100% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05455353 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-926bb4d63826446a99a579960a14c07c |
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| Source note | uspto-grants-1995_10 |
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