HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Hydroxymethylimidazo[5,1-b]thiazole → 5-Formylimidazo[5,1-b]thiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Hydroxymethylimidazo[5,1-b]thiazole | HCID 18359987 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-Formylimidazo[5,1-b]thiazole | HCID 18359938 | 93.1% |
Reaction Steps
To a solution of 480 mg (3.12 mmol) of 5-hydroxymethylimidazo[5,1-b]thiazole in 10 ml of methylene chloride was added 5 g of manganese dioxide, and the mixture was stirred vigorously at room temperature for 2 hours. The reaction solution was filtered through Celite to remove the manganese dioxide. The filtrate was concentrated under reduced pressure to give 442 mg (yield 93%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663162 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-646eb2286d644418ad3cd9a7dccf0573 |
| Source note | uspto-grants-1997_09 |