HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566525Generated: October 25, 2026
Glycolaldehyde → trans-2-Benzoyloxymethyl-5-benzoyl-1,3-oxathiolane
https://huagongshe.com/reaction/566525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycolaldehyde | HCID 756 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 1,4-Dithiane-2,5-diol | HCID 98330 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | trans-2-Benzoyloxymethyl-5-benzoyl-1,3-oxathiolane | HCID 67714070 | 53% |
Reaction Steps
A mixture of glycoaldehyde (1.2 g, 0.01 mol) and mercaptoacetaldehyde dimer (1.52 g, 0.01 mol) in dry pyridine (20 ml) was heated at 90° C. for 2 h. The clear solution was then cooled in an ice-bath to 0° C., followed by adding benzoyl chloride (4.6 ml). The mixture was stirred at room temperature overnight (16 h), and poured into saturated aqueous NaHCO3 solution (100 ml). The product was extracted into methylene chloride (3×100 ml), washed with water (2×100 ml), dried over MgSO4 and filtered. The solvent was removed on an evaporator and the oily residue was purified on silica gel using hexane:EtOAc 9:1 as eluant to give the product (3.65 g) in 53% yield as a mixture of 1:1 cis and trans isomers.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06175008B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-5fd6d70eac5e4c1f9a020405bb877fe4 |
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| Source note | uspto-grants-2001_01 |
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