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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740652Generated: October 26, 2026

Water → 1-(4-Pyridyl)-2,3-bis(methoxycarbonyl)-6,7-dimethoxynaphthalene

https://huagongshe.com/reaction/1740652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethanesulfonic AcidHCID 6395—
ReactantDimethyl maleateHCID 5271565—
Reactant3,4-Dimethoxy-6-(4-pyridyl) hydroxymethylbenzaldehyde dimethylacetalHCID 22007378—
SolventAcetic AcidHCID 176—
SolventTolueneHCID 1140—
Product1-(4-Pyridyl)-2,3-bis(methoxycarbonyl)-6,7-dimethoxynaphthaleneHCID 11728642—

Reaction Steps

To a solution of 3,4-dimethoxy-6-(4-pyridyl)hydroxymethylbenzaldehyde dimethyl acetal (18.4 g) in a mixture of acetic acid (50 ml) and toluene (50 ml) is added maleic acid dimethyl ester (8.64 ml), and the mixture is refluxed for one hour. To the mixture is added methanesulfonic acid (9.33 ml), and the mixture is refluxed for 8 hours while the generated water is removed by using a Dean-stark apparatus. The mixture is cooled to room temperature and concentrated. The residue is dissolved in chloroform, and the pH value thereof is adjusted to pH 8 with an aqueous potassium carbonate solution. The mixture is extracted with chloroform, and the extract is washed, dried, concentrated, and the residue is crystallized from ether to give 1-(4-pyridyl)-2,3-bis(methoxycarbonyl)-6,7-dimethoxynaphthalene (13.5 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05969140
Source datasetuspto-grants-1999_10
ORD IDord-4ac11749fafa46d0a174d2947512cd77
Source noteuspto-grants-1999_10