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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060860Generated: November 2, 2026

Benzoyl Peroxide → 6-(5-Bromomethylnaphthalen-1-yloxy)nicotinonitrile

https://huagongshe.com/reaction/2060860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant6-(5-Methylnaphthalen-1-yloxy)nicotinonitrileHCID 59401312—
SolventCarbon TetrachlorideHCID 5943—
Product6-(5-Bromomethylnaphthalen-1-yloxy)nicotinonitrileHCID 59401311—

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 6-(5-methylnaphthalen-1-yloxy)nicotinonitrile (Preparation 22) (530 mg, 2.04 mmol) in carbon tetrachloride (30 mL) under argon was added N-bromosuccinimide (435 mg, 2.44 mmol) followed by benzoyl peroxide (25 mg, 0.1 mmol). The mixture was heated to 70° C. for 16 h. The reaction mixture was cooled, filtered through celite, and washed with DCM (70 mL). The organic phase was washed with NaHCO3 (30 mL), brine (30 mL) and dried (MgSO4). Solvent was removed in vacuo to give the title compound: RT=3.93 min; m/z (ES+)=341.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08278442B2
Source datasetuspto-grants-2012_10
ORD IDord-0536866a5ef94586961590a36ec47ba2
Source noteuspto-grants-2012_10