HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → 5-(Benzoxazol-2-yl)-2-methyl-1-tert-butylbenzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 2-(2-Tert-butylaminoanilin-5-yl)benzoxazole | HCID 67498414 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(Benzoxazol-2-yl)-2-methyl-1-tert-butylbenzimidazole | HCID 67497923 | 38% |
Reaction Steps
To a solution of 2-(2-tert-butylaminoanilin-5-yl)benzoxazole (see Working Example 29-1) (45.0 mg, 0.160 mmol) in dimethylformamide (2 mL) was added an aqueous solution of acetaldehyde (approx. 90%, 235 μL, 0.480 mmol) and oxone (63.9 mg, 0.104 mmol), and this was stirred at room temperature for 3 hours. After the reaction was complete, aqueous potassium carbonate solution was added, this was filtered and washed with water. The crystals obtained were purified by silica gel column chromatography to yield the title compound (18.2 mg, 38% yield) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829035B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-2c534f3886654c50aba4cc10635778be |
| Source note | uspto-grants-2014_09 |