HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 4-Ethoxycinnamoylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Piperazine, hexahydrate | HCID 120181 | — |
| Reactant | 3-(4-Ethoxyphenyl)prop-2-enoic acid | HCID 295575 | — |
| Reactant | HCID 53411295 | HCID 53411295 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Ethoxycinnamoylpiperazine | HCID 54406104 | 72% |
Reaction Steps
From 11.52 g. of 4-ethoxycinnamic acid and 10.71 g. of thionylchloride was prepared 4-ethoxycinnamoyl chloride, a solution of which in tetrahydrofuran was added gradually to a solution of 23.4 g. of piperazine hexahydrate, 20.67 g. of 47% hydrobromic acid and 90 ml. of ethanol. The resulting mixture was stirred overnight at room temperature and cooled with ice, the forming crystals being filtered off. The filtrate was condensed and treated just as in Reference example 1 to obtain 11.23 g. of the desired product (72% yield). The product was treated with concentrated hydrochloric acid to give the corresponding hydrochloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04189484 |
| Source dataset | uspto-grants-1980_02 |
| ORD ID | ord-ca2480432f94430592653af21a5735a0 |
| Source note | uspto-grants-1980_02 |