HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 22767842, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 10-Chloro-10,11-dihydro-2,8-dimethyl-dibenz[b,f]oxepin | HCID 22767906 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 22767842 | HCID 22767842 | — |
Reaction Steps
0.8 G. of 10-chloro-10,11-dihydro-2,8-dimethyl-dibenz[b,f]oxepin and 0.58 g. of 1-methyl-piperazine are dissolved in 4 ml. of chloroform and heated at reflux for 21 hours. Then, the chloroform is evaporated in vacuo. The residue is partitioned between benzene and aqueous sodium carbonate solution. The benzene solution is extracted with dilute hydrochloric acid. The hydrochloric acid extract is made alkaline with sodium carbonate and extracted with benzene. Thereafter, the benzene extract is washed several times with water, dried over sodium sulfate, evaporated in vacuo, and there is obtained 1-[10,11-dihydro-2,8-dimethyl-dibenz[b,f]oxepin-10-yl]-4-methyl-piperazine, the dihydrochloride of which melts at 197°-198° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04091023 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-b8e746b684ae4d61aed3c2463f1e1928 |
| Source note | uspto-grants-1978_05 |