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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404355Generated: October 30, 2026

Benzoyl Peroxide → HCID 66677293, compound

https://huagongshe.com/reaction/2404355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantPotassium CarbonateHCID 11430—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Chloro-p-toluonitrileHCID 88894—
ReactantSarcosine t-butyl ester hydrochlorideHCID 11252350—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 66677293HCID 6667729374%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 4-methyl-3-chlorobenzonitrile (4.69 g, 31 mmol), N-bromosuccinimide (6.04 g, 34.2 mmol) and benzoyl peroxide (0.750 g, 3.10 mmol) in ACN (20 mL) was heated under reflux for 18 hours. The reaction mixture was diluted with EtOAc and washed with a saturated aqueous solution of Na2CO3 and brine. The organic phase was dried (MgSO4) and concentrated under vacuum. A portion of the residue (1.0 g, 4.34 mmol) was treated with sarcosine tert-butyl ester hydrochloride (1.57 g, 8.69 mmol) and K2CO3 (2.39 g, 17.4 mmol) in dioxane (5 mL). The resulting mixture was heated at 100° C. for 2 hours, and then concentrated under vacuum. The residue was dissolved in a mixture of DCM and water, and then passed through a hydrophobic frit. The solvent was evaporated under vacuum to afford the title compound (0.952 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802704B2
Source datasetuspto-grants-2014_08
ORD IDord-be80ef2838f447fdbae3c7e661c88f57
Source noteuspto-grants-2014_08