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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474482Generated: October 26, 2026

Acetic Anhydride → 4-((5-Methoxymethyl-2-furanyl)methylene)-2-(2-thienyl)-5(4H)-oxazolone

https://huagongshe.com/reaction/1474482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant5-(Methoxymethyl)-2-furaldehydeHCID 74711—
ReactantSodium AcetateHCID 517045—
Reactant((2-Thienylcarbonyl)amino)acetic acidHCID 679227—
SolventWaterHCID 962—
Product4-((5-Methoxymethyl-2-furanyl)methylene)-2-(2-thienyl)-5(4H)-oxazoloneHCID 7523847250.7%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a screw-capped test tube, N-(2-thienylcarbonyl)glycine (56 mg, 0.3 mmol), 5-(methoxymethyl)-2-furancarboxaldehyde (46 mg, 0.3 mmol), sodium acetate (25 mg, 0.3 mmol) and acetic anhydride (0.3 mL) were added. The test tube was sealed, and it was then stirred at an external temperature of 90° C. Three hours later, the temperature of the reaction solution was returned to room temperature, and water (1.5 mL) was then added thereto. The obtained mixture was stirred at the same temperature as described above for 1.5 hours. Thereafter, the precipitated crystal was collected by filtration, and it was washed with water (5 mL) and was then dried under reduced pressure, so as to obtain 44 mg of the above-captioned compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018238B2
Source datasetuspto-grants-2015_04
ORD IDord-78969d70748d4b8eb24d18508aa0bfd7
Source noteuspto-grants-2015_04