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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-Acetylpyrrole | HCID 14079 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-(3,4-Diethoxyphenyl)-4-chloromethylthiazole | HCID 18707278 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(3,4-Diethoxyphenyl)-4-(2-acetyl-1-pyrrolyl)methylthiazole | HCID 18707376 | 24.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06080764 |
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| Source dataset | uspto-grants-2000_06 |
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| ORD ID | ord-23cca9b6ec8e48369c7c9e1a023d75b3 |
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| Source note | uspto-grants-2000_06 |
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