HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenethyl bromide → 4-phenyl-2-(2-phenylethyl)-1(2H)-phthalazinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenethyl bromide | HCID 7666 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Phenyl-1-(2H)-phthalazinone | HCID 219150 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-phenyl-2-(2-phenylethyl)-1(2H)-phthalazinone | HCID 722795 | 95.1% |
Reaction Steps
Eighty-five grams (0.38 moles) of 4-phenyl-1(2H)-phthalazinone was added to 18.4 g (0.47 moles) of sodium hydride in 1 L of DMSO in four portions. The mixture was stirred for two hours at room temperature until evolution of hydrogen had ceased, and 95.5 g (0.52 moles) of 2-bromoethylbenzene was added. The mixture was stirred 1.5 hours at room temperature, 1 L of 2N NaOH was added and the slurry was poured into 1 L of water. The product was filtered off and dried to yield 118 g (95%) of 4-phenyl-2-(2-phenylethyl)-1(2H)-phthalazinone, mp 135-138.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05624922 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-94ea99dcbbe542119c1f3db607b380b9 |
| Source note | uspto-grants-1997_04 |