HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Piperazine, 1-(diphenylmethyl)-4-(2-(1-piperidinylmethyl)-2-propenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 13864639 | HCID 13864639 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Piperazine, 1-(diphenylmethyl)-4-(2-(1-piperidinylmethyl)-2-propenyl)- | HCID 3087340 | — |
Reaction Steps
A mixture of 7.0 g of 1-benzhydryl-4-(2-chloromethyl-2-propenyl)-piperazine (0.0205 mole) and 6.98 g of piperidine (0.082 mole) in 150 ml of absolute ethanol is heated until it has dissolved completely, and subjected to reflux for 3 hours. Then, it is conditioned to room temperature and the ethanol is removed by distillation. The resulting crude reaction product is treated with distilled water several times until a solid material is obtained which is then filtered and washed abundantly with water. By recrystallization from ethanol, 7.4 g crystals of 1-benzhydryl-4-(2-(1-piperidinylmethyl)-2-propenyl)-piperazine (I, R1 =benzhydryl, R2 =2-(1-piperidinylmethyl-2-propenyl) are obtained. Yield: 94%; m.p. 99°-102° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04883797 |
| Source dataset | uspto-grants-1989_11 |
| ORD ID | ord-bfe1f3c6fcb34c69bc4e0b6290cc8d58 |
| Source note | uspto-grants-1989_11 |