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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421983Generated: October 25, 2026

Sodium Iodide → 2-(3,4-Diethoxyphenyl)-4-(2-acetyl-1-pyrrolyl)methylthiazole

https://huagongshe.com/reaction/1421983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant2-AcetylpyrroleHCID 14079—
ReactantSodium HydroxideHCID 14798—
Reactant2-(3,4-Diethoxyphenyl)-4-chloromethylthiazoleHCID 18707278—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(3,4-Diethoxyphenyl)-4-(2-acetyl-1-pyrrolyl)methylthiazoleHCID 1870737624.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

In a mixed solvent consisting of 2 ml of dimethylformamide and 0.2 ml of water were dissolved 200 mg of 2-(3,4-diethoxyphenyl)-4-chloromethylthiazole, 73 mg of 2-acetylpyrrole, 200 mg of sodium iodide and 200 mg of sodium hydroxide. The solution was stirred at 80° C. for 4 hours. The reaction mixture was subjected to distillation to remove the solvent. To the residue were added 30 ml of dichloromethane and 20 ml of water, and phase separation was conducted. The organic layer was washed with 15 ml of a saturated aqueous sodium chloride solution, dried and subjected to distillation to remove the solvent. The residue was recrystallized from methanol to obtain 60 mg of 2-(3,4-diethoxyphenyl)-4-(2-acetyl-1-pyrrolyl)methylthiazole as white acicular crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080764
Source datasetuspto-grants-2000_06
ORD IDord-23cca9b6ec8e48369c7c9e1a023d75b3
Source noteuspto-grants-2000_06