HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl Peroxide → 2-(Bromomethyl)-3,5,6-trimethylpyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Tetramethylpyrazine | HCID 14296 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-(Bromomethyl)-3,5,6-trimethylpyrazine | HCID 13584992 | — |
Reaction Steps
More preferably, dissolving dehydrated tetramethylpyrazine into an organic solvent, preferably CCl4, and adding NBS at a molar ratio of tetramethylpyrazine to NBS=1:0.7, adding a small amount of benzoylperoxide as the radical initiator, reacting with the illumination of an incandescent lamp and reacting for 10-12 h under reflux, then cooling and condensing the reaction liquid, and sucking away the excess tetramethylpyrazine under reduced pressure in 60-70° C. water bath, the residue being kept in a fridge for standing and thus 2-bromomethyl-3,5,6-trimethylpyrazine being obtained as a pale-red half-oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987449B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-fb0fb0c014ed41ceb3065a5f4eb49124 |
| Source note | uspto-grants-2015_03 |