HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992916Generated: October 27, 2026
Hydrochloric Acid → 2,3-Dihydroimidazo[2,1-b][1,3]thiazole-6-carbaldehyde
https://huagongshe.com/reaction/992916
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Ethyl 2,3-dihydroimidazo[2,1-b]thiazole-6-carboxylate | HCID 18183084 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,3-Dihydroimidazo[2,1-b][1,3]thiazole-6-carbaldehyde | HCID 11240604 | 43% |
Reaction Steps
Ethyl 2,3-dihydroimidazo[2,1-b]thiazole-6-carboxylate (4.2 g; 21.21 mmol) was dissolved in dry dichloromethane (150 ml) and cooled to −70° C. under a stream of dry argon. This solution was treated with a solution of diisobutylaluminium hydride in toluene (1.5M, 26.9 ml, 2 equivalents) over 40 minutes at −70° C. The reaction mixture was stirred at −70° C. for a further 0.5 h. Water (10 ml) was added and the mixture stirred at ambient temperature for 0.5 hr. The mixture was acidified with 5M HCl, filtered through a celite pad and the pad further washed with dichloromethane. The combined organic extracts were dried over anhydrous magnesium sulphate and evaporated to dryness. Chromatography on silica gel, eluting with ethyl acetate, gave the title compound (1.4 g, 43%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472383B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-90457985ccc9454da0a5721f10389568 |
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| Source note | uspto-grants-2002_10 |
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