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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1653976Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 15672403, compound

https://huagongshe.com/reaction/1653976

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 numberUS05405827
Source datasetuspto-grants-1995_04
ORD IDord-8eb65450ca524eb1b00214e20cec05a9
Source noteuspto-grants-1995_04