HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Chlorophenyl)piperazine → HCID 20232521, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Chlorophenyl)piperazine | HCID 97478 | — |
| Reactant | 1-(4-(2-Bromoethyl)phenyl)ethan-1-one | HCID 611194 | — |
| Product | HCID 20232521 | HCID 20232521 | 64% |
Reaction Steps
By the reaction of 1-(4-chlorophenyl)-piperazine with 4'-(2-bromoethyl)-acetophenone analogously to Example (41a), there is obtained 4'-{2-[1-(4-chlorophenyl)-piperazin-4-yl]-ethyl}-acetophenone. Yield 64% of theory; m.p. 141°-143° C. (recrystallised from ethyl acetate).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04616086 |
| Source dataset | uspto-grants-1986_10 |
| ORD ID | ord-0cd9bd76e1fb4cee992783f314e98614 |
| Source note | uspto-grants-1986_10 |