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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Mercaptoethanol | HCID 1567 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 2,2-diethoxyethyl Benzoate | HCID 11817258 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1,3-Oxathiolane-2-methanol, 2-benzoate | HCID 11064076 | 91% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08153416B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-3ea92c4ddcb242dd905278dd209fdfed |
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| Source note | uspto-grants-2012_04 |
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