HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 2-(4-Chlorobenzoyl)-quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | p-Bromochlorobenzene | HCID 7806 | — |
| Reactant | Ammonium Bromide | HCID 25514 | — |
| Reactant | Quinoline-2-carbonitrile | HCID 74031 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(4-Chlorobenzoyl)-quinoline | HCID 12495545 | 89% |
Reaction Steps
The starting substance is prepared as follows: 15.4 g (0.1 mole) of 2-cyano-quinoline are dissolved in 200 ml of anhydrous ether, and a Grignard reagent prepared from 2.5 g (0.13 moles) of 4-chloro-bromobenzene and 3.16 g (0.13 moles) of magnesium metal are added. The reaction mixture is allowed to stand overnight, thereafter it is poured into a mixture of 15 g of ammonium bromide and ice, acidified with sulfuric acid and the organic phase is separated. After evaporating the ether the product thus-obtained (24 g) is recrystallized from ethanol. The 2-(4-chlorobenzoyl)-quinoline is obtained with a yield of 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04419355 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-e4db71ac23cb42dfa90d61d08439b931 |
| Source note | uspto-grants-1983_12 |