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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548631Generated: October 30, 2026

1-Methylimidazole → (2-Oxo-1,3-oxazolidin-4-yl)methyl 4-methylbenzene-1-sulfonate

https://huagongshe.com/reaction/548631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylimidazoleHCID 1390—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant4-(Hydroxymethyl)-1,3-oxazolidin-2-oneHCID 14456889—
SolventDichloromethaneHCID 6344—
Product(2-Oxo-1,3-oxazolidin-4-yl)methyl 4-methylbenzene-1-sulfonateHCID 1445689175%

Reaction Conditions

Temperature0 °C

Reaction Steps

N-methylimidazole (360 ml, 4.5 mmol, 1.5 eq) is added to a cooled suspension of 4-(hydroxymethyl)-1,3-oxazolidin-2-one a90 (0.35 g, 3 mmol, 1 eq) in dichloromethane (20 ml). p-Toluenesulfonyl chloride a40 (0.63 g, 3.3 mmol, 1.1 eq) in dichloromethane (5 ml) is then added, dropwise. The mixture is stirred at 0° C. for 5 hours then at room temperature for 24 hours. The mixture is then quenched under vigorous stirring with 0.5 ml of water and taken up in chloroform (100 ml). The organic phase is washed with a saturated aqueous solution of sodium hydrogenocarbonate (2×25 ml), with a 1N solution of hydrochloric acid (2×25 ml), with brine, and is dried over magnesium sulfate. The organic layer is concentrated in vacuo to afford 0.61 g of (2-oxo-1,3-oxazolidin-4-yl)methyl 4-methylbenzenesulfonate a91 as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943605B2
Source datasetuspto-grants-2011_05
ORD IDord-f4ba0346a6fd48c0baec5272191de0e9
Source noteuspto-grants-2011_05