HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 1-(5-bromothiophen-2-yl)-2-methyl-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methylimidazole | HCID 12749 | — |
| Reactant | 2,5-Dibromothiophene | HCID 18453 | — |
| Reactant | L-Proline | HCID 145742 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 1-(5-bromothiophen-2-yl)-2-methyl-1H-imidazole | HCID 67260532 | 31.3% |
Reaction Steps
To the solution of 2,5-dibromothiophene (20 g, 82.6 mmol) and 2-methyl-1H-imidazole (4.1 g, 50 mmol) in DMSO (100 mL) was added CuI (3.14 g, 16.5 mmol), L-proline (0.95 g, 8.3 mmol), K2CO3 (22.9 g, 0.165 mol), the resultant mixture was heated to 100° C. under N2 balloon protection overnight. The reaction mixture was filtrated and the filtrate was poured into water, extracted with EtOAc (300 mL×5). The combined organic layers were washed with brine, dried over Na2SO4, and then filtrated, the filtrate was concentrated under reduced pressure, the residue was purified by column chromatography to give desired 1-(5-bromothiophen-2-yl)-2-methyl-1H-imidazole (3.8 g, yield 31.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08859611B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-dccd881a0092448d903a1bfc98099c65 |
| Source note | uspto-grants-2014_10 |