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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804871Generated: October 30, 2026

Sodium Hydroxide → 2-(4-Methoxy-3-propoxyphenyl)-4-(5-carbonyl-2-furyl)thiazole

https://huagongshe.com/reaction/1804871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1,4-DioxaneHCID 31275—
Reactant2-(4-Methoxy-3-propoxyphenyl)-4-(5-methoxycarbonyl-2-furyl)thiazoleHCID 18511698—
SolventMethanolHCID 887—
Product2-(4-Methoxy-3-propoxyphenyl)-4-(5-carbonyl-2-furyl)thiazoleHCID 8658425847.1%

Reaction Steps

To a suspension of 970 mg of 2-(4-methoxy-3-propoxyphenyl)-4-(5-methoxycarbonyl-2-furyl)thiazole in 30 ml of methanol was added 20 ml of 1,4-dioxane and 5 ml of a 5 N aqueous sodium hydroxide solution. The reaction mixture was refluxed for 3 hours, then concentrated approximately 1/10. Water was added to the residue, and washed with ethyl acetate. To the aqueous layer was acidified with 5 N hydrochloric acid, and extracted with ethyl acetate. The combined organic layer was washed with water and a saturated aqueous sodium chloride solution, and dried with magnesium sulfate. Evaporation the solution, the residue was recrystallized from ethyl acetate to obtain 420 mg of 2-(4-methoxy-3-propoxyphenyl)-4-(5-carbonyl-2-furyl)thiazole as a white powder. mp. 191.0-192.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354439B2
Source datasetuspto-grants-2013_01
ORD IDord-a1e7d7bc0a544513a9119fb36248199c
Source noteuspto-grants-2013_01