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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689573Generated: October 27, 2026

2-Mercaptoethanol → 1,3-Oxathiolane-2-methanol, 2-benzoate

https://huagongshe.com/reaction/1689573

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MercaptoethanolHCID 1567—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant2,2-diethoxyethyl BenzoateHCID 11817258—
SolventTolueneHCID 1140—
Product1,3-Oxathiolane-2-methanol, 2-benzoateHCID 1106407691%

Reaction Steps

To a 5-L, three-necked, round-bottomed flask fitted with a mechanical stirrer, a Dean-Stark apparatus, and a glass stopper is added 2-(benzoyloxy)acetaldehyde diethyl acetal (0.469 mol, 111.85 g, 1.0 equiv.), 2-mercaptoethanol (0.516 mol, 40.34 g, 1.1 equiv.), para-toluenesulfonic acid monohydrate (0.047 mol, 8.92 g, 0.1 equiv.) and toluene (3.5 L). The reaction was heated to reflux and stirred while monitoring progress by TLC. When determined to be complete, the reaction was allowed to cool to ambient temperature before washing with saturated sodium bicarbonate solution. The organic phase was dried over magnesium sulfate and concentrated by rotary evaporation to give (+/−)-2-(benzoyloxymethyl)-1,3-oxathiolane as an oil (95.75 g, 90.9% yield). The crude product was advanced to the next reaction step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153416B2
Source datasetuspto-grants-2012_04
ORD IDord-3ea92c4ddcb242dd905278dd209fdfed
Source noteuspto-grants-2012_04