HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225873Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 15672403, compound
https://huagongshe.com/reaction/2225873
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1,4-Butanediol | HCID 8064 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 15672397 | HCID 15672397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 15672403 | HCID 15672403 | 62% |
Reaction Steps
A solution of 5-formyl-2,3-pyridinedicarboxylic acid, dimethyl ester, 5-dimethyl acetal (1.3 g, 0.0048 mol), a catalytic amount of p-toluenesulfonic acid, 1,4-butanediol and toluene is heated at reflux temperature for 2 hours and 30 minutes. The reaction mixture is cooled to room temperature, made basic with sodium bicarbonate and concentrated in vacuo to give a liquid. The liquid is partitioned between methylene chloride and 5% sodium bicarbonate solution. The layers are separated and the aqueous layer is extracted with methylene chloride, the combined methylene chloride extracts are dried over anhydrous magnesium sulfate and concentrated in vacuo to give an oil. The oil is chromatographed using silica gel and hexanes/ethyl acetate (2:1 to 1:1) as eluant to give the title compound as a clear oil (0.88 g, 62%), identified by IR and NMR spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05344935 |
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| Source dataset | uspto-grants-1994_09 |
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| ORD ID | ord-f71f232bf5a94d76a8a71109b3c03154 |
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| Source note | uspto-grants-1994_09 |
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