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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356833Generated: October 25, 2026

N-bromobutanimide → 2-(1-Naphthyl)benzyl bromide

https://huagongshe.com/reaction/356833

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant(Methylphenyl)naphthaleneHCID 3016790—
CatalystAzobisisobutyronitrileHCID 6547—
SolventCarbon TetrachlorideHCID 5943—
Product2-(1-Naphthyl)benzyl bromideHCID 1107733391.2%

Reaction Steps

114 g (0.52 mol) of 18 and 103 g (0.58 mol) of N-bromo-succinimide were dissolved in 2000 cm3 of tetrachloro-methane at room temperature, 3 g of azobisisobutyronitrile were added, and the mixture was refluxed for 4 hours. The succinimide which precipitated was filtered off, the solvent was removed in vacuo, and the residue was purified by filtration through 1000 g of silica gel (hexane/methylene chloride 9:1), giving 141 g (82%) of 19 as a colorless lachrymatory oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840644
Source datasetuspto-grants-1998_11
ORD IDord-11e0ec7f017a45db8fc648a77f1da37c
Source noteuspto-grants-1998_11