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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875047Generated: November 3, 2026

Azobisisobutyronitrile → 1-{[3-(Bromomethyl)-6-chloro-2-fluorophenyl]oxy}naphthalene

https://huagongshe.com/reaction/1875047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant1-[(6-Chloro-2-fluoro-3-methylphenyl)oxy]naphthaleneHCID 68488277—
SolventCarbon TetrachlorideHCID 5943—
Product1-{[3-(Bromomethyl)-6-chloro-2-fluorophenyl]oxy}naphthaleneHCID 6848555845.5%

Reaction Steps

To a solution of 1-[(6-chloro-2-fluoro-3-methylphenyl)oxy]naphthalene (1.69 g, 5.89 mmol) in carbon tetrachloride (20 mL) was added N-bromosuccinimide (1.154 g, 6.48 mmol) and AIBN (0.048 g, 0.295 mmol). The mixture was heated at reflux overnight. The reaction mixture was filtered through Celite and the solvent was evaporated. The residue was purified by flash chromatography (hexane:ethyl acetate) to give the desired product (0.98 g, 45.5%) as a light yellow oil. 1H NMR (400 MHz, chloroform-d) δ ppm 8.43-8.51 (m, 1H), 7.84-7.92 (m, 1H), 7.53-7.64 (m, 3H), 7.23-7.34 (m, 3H), 6.50 (d, 1H), 4.50 (d, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304419B2
Source datasetuspto-grants-2012_11
ORD IDord-aedcfd401bbe4b488797dda86d99bc54
Source noteuspto-grants-2012_11