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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843484Generated: October 31, 2026

Azlactone → HCID 18551976, compound

https://huagongshe.com/reaction/843484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzlactoneHCID 65073—
Reactant3-Methoxy-2-nitropyridineHCID 556063—
ReactantSodium Carbonate MonohydrateHCID 2735133—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 18551976HCID 18551976—

Reaction Steps

A solution of Na2CO30.10 H2O Na2CO3.10 H2O (7.3 mmol) in H2O (10 ml) is emulsified under vigorous stirring at about room temperature or slightly elevated temperature with a solution of 2-nitro-3-methoxypyridine (4.25 mmol) and tetrabutylammonium bromide (10.06 mmol) as phase transfer catalyst in methylene chloride (˜20 mL). 2-phenyl-5(4H)-oxazolone (˜60 mmol) is added in several portions during one hour. The layers are separated and the aqueous phase is washed with CH2Cl2. The combined organic solutions are dried with Na2SO4 and is are evaporated under reduced pressure. The residue is chromatographed in silica gel starting with petroleum ether to which methylene chloride is gradually added. After recrystallizing, the complex is placed in refluxing methanol to which a catalytic amount of p-toluene sulfonic acid has been added. The sample is refluxed overnight. After cooling and evaporation of the solvent, the above-identified product is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037686E1
Source datasetuspto-grants-2002_04
ORD IDord-00f29a3b10874d9faf12a80ae74216e7
Source noteuspto-grants-2002_04