HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-{4-[5-Bromo-3-(tert-butyl)-2-methoxyphenyl]piperazino}acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | 1-(5-Bromo-3-(tert-butyl)-2-methoxyphenyl]piperazine | HCID 58909960 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-{4-[5-Bromo-3-(tert-butyl)-2-methoxyphenyl]piperazino}acetonitrile | HCID 58910031 | 78% |
Reaction Steps
1-[5-bromo-3-(tert-butyl)-2-methoxyphenyl]piperazine (550 mg), potassium carbonate (302 mg), dimethylformamide (7 ml) and bromoacetonitrile (0.12 ml) were combined and the mixture was stirred at room temperature for 4 hours. The reaction mixture was diluted with ethyl acetate, the insoluble portion was filtered off, and the concentrated residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (480 mg) as colorless crystals (78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244730B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-91fa5a39439f45648d3494508a4e872e |
| Source note | uspto-grants-2007_07 |