HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Bromochlorobenzene → 3-(4-Chlorobenzoyl)-isoquinoline imine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Isoquinolinecarbonitrile | HCID 5076808 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-(4-Chlorobenzoyl)-isoquinoline imine | HCID 2825604 | 60% |
Reaction Steps
The starting substance is prepared as follows: To a mixture of 0.62 g (26 millimoles) of metallic magnesium and 8 ml of anhydrous ether a solution of 5.0 g (26 millimoles) of 4-chloro-bromobenzene in ether is dropwise added, the Grignard solution thus-obtained is admixed with 3.1 g (20 millimoles) of 3-cyano-isoquinoline, and the reaction mixture is stirred at room temperature for an hour. The Grignard complex is decomposed with an ammonium chloride solution, the solvent is distilled off and the residue is recrystallized from ethanol. 3.2 g (60%) of 3-(4-chlorobenzoyl)-isoquinoline imine are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04419355 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-a0bc1ef5934a47d78fc695e65761307f |
| Source note | uspto-grants-1983_12 |