HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566524Generated: October 26, 2026
Glycolaldehyde → trans-2-Acetoxymethyl-5-acetoxy-1,3-oxathiolane
https://huagongshe.com/reaction/566524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Glycolaldehyde | HCID 756 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1,4-Dithiane-2,5-diol | HCID 98330 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | trans-2-Acetoxymethyl-5-acetoxy-1,3-oxathiolane | HCID 69945247 | 59% |
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 acetyl chloride (2.8 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 hexane:EtOAc 9:1 as eluant to give the product (2.8 g) in 59% yield as a mixture of 1:1 cis: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-bf3d8002e26a46769f34eb6d3fb4c9a8 |
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| Source note | uspto-grants-2001_01 |
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