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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650969Generated: October 26, 2026

4-Toluenesulfonyl chloride → ((5R)-2-oxo-1,3-oxazolidin-5-yl)methyl4-methylbenzenesulfonate

https://huagongshe.com/reaction/650969

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant(5R)-5-(hydroxymethyl)-1,3-oxazolidin-2-oneHCID 10236003—
ReactantSodium chloride dihydrateHCID 23713072—
SolventPyridineHCID 1049—
Product((5R)-2-oxo-1,3-oxazolidin-5-yl)methyl4-methylbenzenesulfonateHCID 2793763—

Reaction Steps

A solution of (5R)-5-(hydroxymethyl)-1,3-oxazolidin-2-one (10.0 g), prepared as described in Tetrahedron: Asymmetry 1995, 6, 1181-1190, in pyridine (60 mL) at −10° C. was treated with para-toluenesulfonyl chloride (21.2 g), stirred for 2 hours, poured into 1:1 brine/water (100 mL), and extracted with ethyl acetate. The extract was washed with 1:1 saturated sodium bicarbonate/water and 1:1 brine/water, and the washes were back extracted with ethyl acetate. The combined extracts was dried (MgSO4), filtered, and concentrated to provide the desired product. MS (ESI(+)) m/e 272 (M+H)+; 1H NMR (300 MHz, CDCl3) δ 7.80 (d, 2H), 7.39 (d, 2H), 4.80 (m, 1H), 4.18 (d, 2H), 3.70 (t, 1H), 3.50 (dd, 1H), 2.45 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277868B1
Source datasetuspto-grants-2001_08
ORD IDord-5c581483aa0943ae8a4be73ea380bc95
Source noteuspto-grants-2001_08