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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53827Generated: October 29, 2026

N-bromobutanimide → 6-Bromomethyl-2(2'-cyanophenyl)-naphthalene

https://huagongshe.com/reaction/53827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant6-Methyl-2-(2'-cyanophenyl)-naphthaleneHCID 21848056—
SolventCarbon TetrachlorideHCID 5943—
Product6-Bromomethyl-2(2'-cyanophenyl)-naphthaleneHCID 21848062—

Reaction Steps

A mixture of 6.30 g of 6 g of 6-methyl-2-(2'-cyanophenyl)-naphthalene, 4.60 g of N-bromosuccinimide and 0.085 g of azoisobutyronitrile in 70 ml of carbon tetrachloride is heated at 110° for 4 hours. The cooled reaction mixture is extracted twice with 45 ml of 2N sodium hydroxide solution each time. The aqueous phases are then extracted with 50 ml of CH2Cl2 in each case. The combined organic phases are dried over MgSO4. After removing the solvent in vacuo, the crude product is recrystallised from toluene/hexane and yields 6-bromomethyl-2(2'-cyanophenyl)-naphthalene, m.p. 171°-172°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620998
Source datasetuspto-grants-1997_04
ORD IDord-29ffdc87a0eb4c10b97df8e56f2bddfe
Source noteuspto-grants-1997_04