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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111099Generated: October 31, 2026

Benzoyl Peroxide → HCID 14637615, compound

https://huagongshe.com/reaction/1111099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantTetramethylpyrazineHCID 14296—
ReactantChlorosuccinimideHCID 31398—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 14637615HCID 14637615—

Reaction Conditions

Temperature0 °C

Reaction Steps

A reaction mixture containing N-chlorosuccinimide (6.67 g, 50.0 mmol), benzoylperoxide (50 mg) and TMPZ (6.81 g, 50.0 mmol), in 125 ml of reagent grade CCl4 was refluxed for 12 hours. The reaction solution was then cooled to 0° C. and filtered, removing succinimide. The solvent was evaporated in vacuo resulting in an oil (chloromethyltrimethylpyrazine). The oil was cooled to 0° C. and 25 ml of distilled n-amyl amine was dripped into the oil over a 20 minute period. The reaction mixture was stirred in an ice bath until an exothermic reaction ensured whereby the mixture was gently refluxed for 5 hours. Upon filtration of this reaction mixture, the resulting oil was chromatographed by flash column chromatography using 230-400 mesh silica gel (available from Fisher Scientific Co., King of Prussia, Pa.). Fractional separation was obtained by using a gradient solvent system (100% CHCl3 →25:1 CDCl3 /MeOH+1% NH4OH). Purification by Kugelrohr distillation at 90° C./15 mm Hg afforded 15% yield of a clear oil. m.p. 174°-175° C. Analysis: H-NMR(CDCl3) (ppm): 3.8(2H,S), 2.6-2.7(2H,t), 2.45-2.5(9H,t), 1.8-1.9(2H,m), 1.5-1.6(2H,m), 1.3-1.37(4H, sextet), 0.8-0.9(3H,t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04978662
Source datasetuspto-grants-1990_12
ORD IDord-5dfca3bc636649949952bddbc3a728d1
Source noteuspto-grants-1990_12