HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phthalazine → HCID 21814495, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phthalazine | HCID 9207 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21814495 | HCID 21814495 | — |
Reaction Steps
A solution of 4 g of phthalazine in 50 ml of tetrahydrofuran is added dropwise at room temperature to a solution of phenyl-magnesium bromide (prepared from 6 g of bromobenzene and 1 g of magnesium in 30 ml of tetrahydrofuran). The reaction mixture is held at reflux for 6 hrs. After cooling the mixture is treated with a saturated aqueous solution of ammonium chloride and extracted 3 times with diethyl ether. The organic phases are combined, dried and subsequently triturated with pentane. 2.32 g of not quite pure 1-phenyl-1,2-dihydro-phthalazine are isolated as a yellowish solid, m.p. 79° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06114330 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-f347a3885e3a44f0b5559b46af346e0f |
| Source note | uspto-grants-2000_09 |