HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 4-(Dibromomethyl)biphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | 4-Methylbiphenyl | HCID 12566 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1,1'-Biphenyl, 4-(bromomethyl)- | HCID 257716 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(Dibromomethyl)biphenyl | HCID 11244269 | — |
Reaction Steps
4-(Bromomethyl)biphenyl: A mixture of 4-phenyltoluene (4.83 g, 28.7 mmol), N-bromosuccinimide (5.64 g, 31.7 mmol), benzoyl peroxide (catalytic), and anhydrous carbon tetrachloride (35 mL) was refluxed for 24 hours. The mixture was coofed to room temperature and filtered to give a mixture (7.32 g) of 4-(dibromomethyl)biphenyl, 4-(bromomethyl)biphenyl, and 4-phenyltoluene (14:82:4 molar ratio by 1H-NMR). The product was used without further purification in the next step. 1H-NMR of the title compound (300 MHz, CDCl3) δ 7.56-7.60 (m, 4H), 7.33-7.48 (m, 5H), 4.55 (s, 2H). Partial 1H-NMR of 4-(dibromomethyl)biphenyl (300 MHz, CDCl3) δ 6.71 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06518310B2 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-381dfbefb93142baa63f5acfd97438ae |
| Source note | uspto-grants-2003_02 |