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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225873Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 15672403, compound

https://huagongshe.com/reaction/2225873

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant1,4-ButanediolHCID 8064—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 15672397HCID 15672397—
SolventTolueneHCID 1140—
ProductHCID 15672403HCID 1567240362%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05344935
Source datasetuspto-grants-1994_09
ORD IDord-f71f232bf5a94d76a8a71109b3c03154
Source noteuspto-grants-1994_09