HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 2-Methyl-3-bromo-3-phenyloctan-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methyl-3-phenyloctan-4-one | HCID 59864985 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Methyl-3-bromo-3-phenyloctan-4-one | HCID 59864941 | — |
Reaction Steps
To a magnetically stirred solution of 2-methyl-3-phenyloctan-4-one (Intermediate IIa-1) (4.31 gram, 0.02 mol) in CCl4 (40 ml) was added a catalytic amount of dibenzoyl peroxide and NBS (6.56 gram). The resulting mixture was heated for 6 hours at reflux temperature. The obtained mixture was allowed to attain room temperature. The formed precipitate was removed by filtration. The filtrate was concentrated to give crude 2-methyl-3-bromo-3-phenyloctan-4-one (intermediate IIb-1)—contaminated with some starting material—as a dark-colored oil (6.77 gram). 1H-NMR (400 MHz, CDCl3) Characteristic signals: δ 0.68 (d, J=6, 3H), 0.78 (t, J=7, 3H), 1.08 (d, J=6, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410135B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-d56faf7de1984d74a32513b4c5ce36b3 |
| Source note | uspto-grants-2013_04 |