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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250320Generated: October 30, 2026

Azobisisobutyronitrile → 7-(Bromomethyl)-2-naphthonitrile

https://huagongshe.com/reaction/1250320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant7-Methyl-2-naphthalenecarbonitrileHCID 9815323—
SolventIsobutyronitrileHCID 6559—
Product7-(Bromomethyl)-2-naphthonitrileHCID 983774858.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

2,2′-azobisisobutyronitrile (491 mg, 3 mmol) and isobutyronitrile (50 ml) were added to 7-methyl-2-naphthalene carbonitrile (5.0 g, 30 mmol) at room temperature. N-bromosuccinimide (5.3 g, 30 mmol) was added thereto, and the mixture was heated at an internal temperature of 80° C. for 2 hours. After that, the experiment was conducted in the same way as Example 12. Analysis by reversed-phase chromatography by use of the obtained product from Example 11 as a standard sample revealed that 4.3 g of the title compound was obtained (58% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06337405B1
Source datasetuspto-grants-2002_01
ORD IDord-8d09dd0b37fb4f469c8ffc1757535b7b
Source noteuspto-grants-2002_01