HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444163Generated: October 26, 2026
Potassium Hydroxide → 2-Bromoimidazo(4,3-b)(1,3)thiazole-7-carboxylic acid
https://huagongshe.com/reaction/1444163
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 2-bromoimidazo[5,1-b]thiazole-7-carboxylate | HCID 59168405 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 2-Bromoimidazo(4,3-b)(1,3)thiazole-7-carboxylic acid | HCID 59168404 | 91.1% |
Reaction Steps
A 2 M aqueous solution (35 ml) of potassium hydroxide was added to ethyl 2-bromoimidazo[5,1-b] thiazole-7-carboxylate (1.32 g, 4.80 mmol), and the mixture was stirred at 60° C. for one hr. After the completion of the reaction, the reaction solution was poured into 4 M hydrochloric acid (20 ml) under ice cooling to precipitate a solid. The resultant solid was washed with water, and a mixed solvent composed of ethanol and toluene was added thereto. The solvent was removed by distillation under the reduced pressure, and the residue was then dried to give 2-bromoimidazo[5,1-b]thiazole-7-carboxylic acid (1.08 g, 91%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07662841B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-c7f5ef9954ae4a4aa9ac44f5e911798b |
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| Source note | uspto-grants-2010_02 |
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