HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine Dihydrochloride → Methyl 4-[(piperazin-1-yl)methyl]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine Dihydrochloride | HCID 8893 | — |
| Reactant | Piperazine, hexahydrate | HCID 120181 | — |
| Reactant | Methyl 4-(bromomethyl)benzoate | HCID 256687 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 4-[(piperazin-1-yl)methyl]benzoate | HCID 7018627 | 64% |
Reaction Steps
A mixtue of 38 g. (0.2 mole) piperazine hexahydrate, 28 g. (0.2 mole) piperazine dihydrochloride and 150 ml. methanol is mixed, while stirring at ambient temperature, with 45 g. (0.2 mole) methyl 4-bromomethylbenzoate. The reaction mixture is left to stand for 2 days and suction filtered from the precipitate. The clear solution is evaporated and the residue is recrystallised from ethanol to give 39 g. (64%) of the desired compound as a monohydrochloride; m.p. 226°-227° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04616086 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-c2a1209efed14541a56982e6500c44bc |
| Source note | uspto-grants-1986_10 |