HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 1,1'-Biphenyl, 4'-(bromomethyl)-2-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4'-Methyl-2-nitro-1,1'-biphenyl | HCID 10443194 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 1,1'-Biphenyl, 4'-(bromomethyl)-2-nitro- | HCID 11779072 | 92.1% |
Reaction Steps
A solution/suspension of 3.74 g (17.5 mmol) 2-nitro-4'-methylbiphenyl, 123 mg (0.9 mmol) AIBN, and 3.43 g (19.3 mmol) NBS in 180 mL CCl4 was refluxed for 30 minutes. The mixture was cooled to room temperature, was filtered through a medium fritted funnel, was washed with water, was dried over magnesium sulfate, was stripped of solvent in vacuo, and was chromatographed on silica gel under medium pressure using 7% ethyl acetate in hexanes to give 4.71 g (92% yield) of the title compound as a light yellow crystalline solid. Rf 0.21 in 10% EtOAc/hexane, visualized by UV and ammonium molybdate/ceric sulfate stain.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250521 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-c5952f2b9ae747d782b14d29b14f9e3f |
| Source note | uspto-grants-1993_10 |