HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(3-Chlorophenyl)piperazine → 1-Piperazineacetic acid, 4-(3-chlorophenyl)-α-methyl-, ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(3-Chlorophenyl)piperazine | HCID 1355 | — |
| Reactant | Ethyl Acrylate | HCID 8821 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Piperazineacetic acid, 4-(3-chlorophenyl)-α-methyl-, ethyl ester | HCID 61721311 | — |
Reaction Steps
Over a period of 40 minutes, 108 ml of ethyl acrylate are added to 38.3 g of N-(3-chlorophenyl)piperazine dissolved in 300 ml of anhydrous ethanol and 0.5 ml of Triton B. The temperature reaches 40° C. when addition is complete. After heating at reflux for 3 hours, the reaction mixture is concentrated in vacuo and the residue is distilled. 139 g of 4-(3-chlorophenyl)piperazin-1-ylpropionic acid ethyl ester are obtained, b.p/0.33 mmHg=176°-179° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04711885 |
| Source dataset | uspto-grants-1987_12 |
| ORD ID | ord-245179c9bc514222afcc1bbbd1aa7586 |
| Source note | uspto-grants-1987_12 |