HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Bromide → HCID 59846088, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 67158336 | HCID 67158336 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59846088 | HCID 59846088 | — |
Reaction Steps
A mixture of 1-(piperidin-3-ylcarbonyl)-4-[3-(trifluoromethyl)phenyl]piperazine hydrochloride (600 mg) in N,N-dimethylformamide (10 ml) was stirred at room temperature. Potassium carbonate (800 mg) was added followed by ethyl bromide (158 mg) and the mixture was stirred overnight. The mixture was filtered through a sinter and then through a SCX-2 column eluting with methanol and then a 7M solution NH3 in methanol. The basic fraction was concentrated at reduced pressure. This gave 1-[(1-ethylpiperidin-3-yl)carbonyl]-4-[3-(trifluoromethyl)phenyl]piperazine as a colourless oil (420 mg)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943768B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-d68f48b892064baa9eae2ed82b0b9054 |
| Source note | uspto-grants-2011_05 |