HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → 1-Piperazinecarboxylic acid, 4-phenyl-, phenylmethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Hexane | HCID 8058 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 1-Piperazinecarboxylic acid, 4-phenyl-, phenylmethyl ester | HCID 9879254 | — |
Reaction Steps
A solution of 4.4 g of benzyl chloroformate in toluene is added to a solution comprising 4.05 g of N-phenylpiperazine in 50 cm3 of benzene and 2.5 g of triethylamine, at a temperature between +5° C. and +10° C. The whole is allowed to return to ambient temperature and agitated for 2 hours. The triethylamine chloride is filtered off and evaporated to dryness. An oily residue is obtained which is solidified in n-hexane and 7.1 g of expected product is recovered. m.p.=49°-51° C. After recrystallization from an ethyl ether -n-hexane mixture, m.p.=51°-52° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05081130 |
| Source dataset | uspto-grants-1992_01 |
| ORD ID | ord-a43f6a1555a54d77b0f5d6de0928ea06 |
| Source note | uspto-grants-1992_01 |