HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989833Generated: October 30, 2026
Benzoyl chloride → 7-Benzoylimidazo[5,1-b]thiazole
https://huagongshe.com/reaction/989833
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Imidazo[5,1-b]thiazole | HCID 21262404 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | 7-Benzoylimidazo[5,1-b]thiazole | HCID 22632056 | — |
Reaction Steps
Aluminum chloride (5.33 g) was added to a solution of 4.64 ml of benzoyl chloride in 50 ml of carbon disulfide. A solution of 1.24 g of imidazo[5,1-b]thiazole in 50 ml of dichloromethane was added dropwise thereto. The mixture was stirred at room temperature for 2 hr. The reaction solution was poured into 50 g of ice. Dichloromethane (100 ml) was added thereto. Sodium carbonate (16.7 g) and 16.7 g of sodium sulfate were added in that order to the mixture with stirring. The insolubles were removed by filtration through Celite, and then washed with dichloromethane. Filtrate was concentrated under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=5:1 to dichloromethane:ethyl acetate=2:1) to give 1.39 g of 7-benzoylimidazo[5,1-b]thiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458780B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-4df208c0b2214a6ba60b4c28c35a3437 |
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| Source note | uspto-grants-2002_10 |
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