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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 633774Generated: October 30, 2026

Benzoyl Peroxide → 2-(Bromomethyl)-3,5,6-trimethylpyrazine

https://huagongshe.com/reaction/633774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantTetramethylpyrazineHCID 14296—
ReactantN-bromobutanimideHCID 67184—
SolventCarbon TetrachlorideHCID 5943—
Product2-(Bromomethyl)-3,5,6-trimethylpyrazineHCID 13584992—

Reaction Steps

More preferably, dehydrated tetramethylpyrazine is dissolved into an organic solvent, preferably CCl4, and then NBS is added at a mole ratio of tetramethylpyrazine to NBS=1:0.7. Then a small amount of benzoylperoxide is added as the radical initiator. The reaction is carried out under the illumination of an incandescent lamp and the reaction liquid is refluxed to react for 10-12 h. Next the reaction liquid is cooled and condensed, and the excess tetramethylpyrazine is sucked away under reduced pressure in 60-70° C. water bath. The residue is kept in a fridge for standing, and 2-bromomethyl-3,5,6-trimethyl pyrazine is obtained as a pale-red half-oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321804B2
Source datasetuspto-grants-2016_04
ORD IDord-4c994169615342248c52676934988c64
Source noteuspto-grants-2016_04