HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444184Generated: October 26, 2026
Toluene → 2-Bromo-7-hydroxymethylimidazo[5,1-b]thiazole
https://huagongshe.com/reaction/1444184
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Ethyl 2-bromoimidazo[5,1-b]thiazole-7-carboxylate | HCID 59168405 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-7-hydroxymethylimidazo[5,1-b]thiazole | HCID 59168406 | 99% |
Reaction Steps
A solution of ethyl 2-bromoimidazo[5,1-b] thiazole-7-carboxylate (101 mg, 0.37 mmol) in dichloromethane (5 ml) was cooled to −50° C. A toluene solution of diisobutylaluminium hydride (1.01 M solution; 1.1 ml, 1.1 mmol) was then added dropwise to the cooled solution, and the mixture was stirred at the same temperature for 10 min. After the completion of the reaction, a saturated aqueous potassium sodium tartrate solution was added thereto, and the mixture was stirred at room temperature for one hr and was extracted with ethyl acetate (7 ml×3). The organic layer was washed with saturated brine and was dried over anhydrous sodium sulfate, and the solvent was removed by distillation under the reduced pressure to give 2-bromo-7-hydroxymethylimidazo[5,1-b]thiazole (85 mg, 99%) 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-b9e31d92e2654e489578c86435f03f29 |
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| Source note | uspto-grants-2010_02 |
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