HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dihydro-6hydroxymethylimidazo[2,1-b]thiazole → 2,3-Dihydroimidazo[2,1-b][1,3]thiazole-6-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dihydro-6hydroxymethylimidazo[2,1-b]thiazole | HCID 18183082 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2,3-Dihydroimidazo[2,1-b][1,3]thiazole-6-carbaldehyde | HCID 11240604 | — |
Reaction Steps
2,3-Dihydro-6-hydroxymethylimidazo[2,1-b]thiazole (1.47 g, 9.4 mmol) was dissolved in acetonitrile (30 ml) by addition of water (minimum volume). Manganese dioxide (4.41 g, 3 wt. equivalents) was added and the mixture stirred at ambient temperatures for 1.5 h. The mixture was filtered through Keiselguhr, the filter pad washed with water and the combined filtrate and washings evaporated to dryness under reduced pressure. The residue was triturated under diethyl ether, the solid collected by filtration and dried in air (1.33 g, 92%); nmax (CH2Cl2) 1685, 1528, 1272, 1260 and 1152 cm−1; dH (90 MHz; CD3OD) 3.84-4.10 (2H, m), 4.20-4.50 (2H, m), 7.97 (1H, s), 9.52 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06472383B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-4b58860e7c864f82ae0aab02761da7ff |
| Source note | uspto-grants-2002_10 |