HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248246Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 15672405, compound
https://huagongshe.com/reaction/2248246
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1,1-Ethanedithiol | HCID 33645 | — |
| Reactant | HCID 15672397 | HCID 15672397 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 15672405 | HCID 15672405 | 67% |
Reaction Steps
A solution of dimethyl 5-formylpyridine-2,3-dicarboxylate (0.73 g, 0.00327 mol), ethanedithiol (0.357 mL, 0.00425 mol) and a catalytic amount of para-toluenesulfonic acid in chloroform (20 mL) is heated at reflux for 5.5 hours. During this time, water is removed by placement of an addition funnel containing 3 angstrom molecular sieves in between the reaction flask and the reflux condensor. After cooling, the reaction is diluted with methylene chloride (20 mL) and is washed with 10% aqueous sodium carbonate and saturated sodium chloride solutions. The organic solution is dried over anhydrous magnesium sulfate and concentrated in vacuo to give a residue. The residue is purified by chromatography using silica gel and 33% ethyl acetate in hexanes as eluant to yield the title compound as a clear oil (0.66 g, 67%), identified by IR and NMR spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05039333 |
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| Source dataset | uspto-grants-1991_08 |
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| ORD ID | ord-c67e73ff1a504f6fbd0cc221eeb2c348 |
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| Source note | uspto-grants-1991_08 |
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