HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Bromo-1-[4-(2,3-dimethylphenyl)piperazin-1-yl]ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromoacetyl bromide | HCID 61147 | — |
| Reactant | 1-(2,3-Dimethylphenyl)piperazine hydrochloride | HCID 13034647 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-1-[4-(2,3-dimethylphenyl)piperazin-1-yl]ethanone | HCID 19066220 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
1-(2,3-Xylyl)piperazine hydrochloride (5 g; 25 mmol) is suspended in dichloromethane and triethylamine (7.6 ml; 54 mmol) is added. The mixture is cooled to 0° C. and bromoacetyl bromide (2.4 ml; 27 mmol) is added dropwise. The reaction is stirred for 30 minutes and then diluted in dichloromethane, washed with half-saturated sodium bicarbonate solution and dried over magnesium sulfate. The final product is purified by flash chromatography with a gradient of eluents (30/70 to 50/50; EtOAc-Pet. ether).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05789412 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-809c495d128f43c7898185415d4eddee |
| Source note | uspto-grants-1998_08 |