HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Benzyl 4-(4-bromophenyl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | 1-(4-Bromophenyl)piperazine | HCID 2735629 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzyl 4-(4-bromophenyl)piperazine-1-carboxylate | HCID 46739494 | — |
Reaction Steps
5 g of 4-bromophenylpiperazine are placed in a 500 ml three-necked flask under a nitrogen atmosphere. 4.34 ml of triethylamine are added. The mixture is cooled in an ice bath and 3.24 ml of benzyl chloroformate are added. The mixture is allowed to return to ambient temperature. It is diluted with dichloromethane and then gentle hydrolysis is carried out. The aqueous phase is extracted with dichloromethane. The organic phases are combined, washed with a saturated NaCl solution, dried over sodium sulphate, then filtered through a sintered glass filter and concentrated under vacuum. 8.43 g of 4-(4-bromophenyl)piperazine-1-carboxylic acid benzyl ester are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08530657B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-c53fbf5f16654f649222fece5a7bfb47 |
| Source note | uspto-grants-2013_09 |