HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → {4-[2-(6-Methoxynaphthalen-2-yl)propyl]piperazin-1-yl}(phenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | HCID 3055305 | HCID 3055305 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | {4-[2-(6-Methoxynaphthalen-2-yl)propyl]piperazin-1-yl}(phenyl)methanone | HCID 3055311 | — |
Reaction Steps
Benzoyl chloride (0.58 ml, 5 mmols) is added, at 0° C., to a solution of 2-(2-piperazino-1-methylethyl)-6-methoxynaphthalene (1.42 g, 5 mmols) and N-ethylmorpholine (0.65 ml, 5 mmols) in 15 ml of methylene chloride. The mixture is allowed to return to ambient temperature and stirred for 3 hours. The reaction medium is washed with water and dried over sodium sulphate. Concentration of the mixture yields an oily residue which dissolves in ether and crystallises. The compound is recrystallised from ethyl acetate (15 ml).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04243665 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-3465046ca378426fa6c710e55f2cf957 |
| Source note | uspto-grants-1981_01 |