HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 1-{4-[5-Bromo-3-(tert-butyl)-2-methoxyphenyl]piperazino}-1-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(5-Bromo-3-(tert-butyl)-2-methoxyphenyl]piperazine | HCID 58909960 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-{4-[5-Bromo-3-(tert-butyl)-2-methoxyphenyl]piperazino}-1-ethanone | HCID 58909995 | 81% |
Reaction Steps
Acetyl chloride (0.10 ml) was mixed with a solution of 1-[5-bromo-3-(tert-butyl)-2-methoxyphenyl]piperazine (370 mg) and triethylamine (0.32 mL) in methylene chloride (8 ml), and the mixture was stirred at room temperature for 3 hours. The reaction mixture was diluted with ethyl acetate and, after filtering off the insoluble portion, was concentrated. The residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (338 mg) as colorless crystals (81%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07244730B2 |
| Source dataset | uspto-grants-2007_07 |
| ORD ID | ord-fc53ad246b67416bbc5f32affe9fb1e8 |
| Source note | uspto-grants-2007_07 |