HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-1-(4-hydroxyphenyl)ethanone → 2-(4-Diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-1-(4-hydroxyphenyl)ethanone | HCID 4964 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-(4-Diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanone | HCID 10340129 | 84.6% |
Reaction Steps
2.52 g (10 mmol) of 1-diphenylmethylpiperazine and 1.11 g (11 mmol) of triethylamine were dissolved in 30 ml of isopropanol, followed by addition of a solution obtained by dissolving 2.15 g (10 mmol) of α-bromo-p-hydroxyacetophenone in 20 ml of isopropanol. The mixture was allowed to stand overnight at room temperature. Precipitated crystals were collected by filtration. The crystals were successively washed with isopropanol, water and isopropanol and then dried to give 3.27 g of crude crystals of 2-(4-diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanone (yield: 84.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04528194 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-80beec8bb1a84b579b1dfbd3da8dfa71 |
| Source note | uspto-grants-1985_07 |