HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 7-(Bromomethyl)-4-chloroquinoline-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Chloro-7-methylquinoline-2-carbonitrile | HCID 59774919 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-(Bromomethyl)-4-chloroquinoline-2-carbonitrile | HCID 66789524 | 57.6% |
Reaction Steps
4-Chloro-7-methyl-2-quinolinecarbonitrile (1-5, 57 g, 0.37 mol, 1.0 equiv.), NBS (75 g, 0.42 mol, 1.14 equiv.) and benzoyl peroxide (0.8 g, 3.3 mmol, 0.01 equiv.) were stirred in CH3CN (30 ml, 12.3 M) at room temperature. After 16 h, the solvent was removed and the residue was partitioned between AcOEt and water, the organic layer was washed with water, dried over MgSO4 and filtered. After removal of the solvent, the residue was recrystallized from methanol to give 60 g of desired 7-(bromomethyl)-4-chloroquinoline-2-carbonitrile (2-4). LRMS m/z (M+H)+ 283.1 found, 282.9 required.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09278960B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-8372bf4412b942e7af1e3ec5bd4c880d |
| Source note | uspto-grants-2016_03 |