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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942631Generated: October 25, 2026

Hydrogen Bromide → 5-Bromo-2-(2-methylpropyl)benzonitrile

https://huagongshe.com/reaction/1942631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Amino-2-(2-methylpropyl)benzonitrileHCID 22227932—
ReactantSodium NitriteHCID 23668193—
Catalystcopper(I) bromideHCID 24593—
CatalystCopper bromide (CuBr2)HCID 24611—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product5-Bromo-2-(2-methylpropyl)benzonitrileHCID 51358165—

Reaction Steps

To a solution of 5-amino-2-isobutylbenzonitrile (D57) (34 g) in acetonitrile (500 mL) was added HBr (24.37 mL) at 0° C. Then a solution of sodium nitrite (16.16 g) in water (50 mL) was added to the reaction mixture. After stirring for 30 min, copper(II) bromide (87 g) and copper(I) bromide (5.60 g) were added to the reaction mixture. The mixture was stirred at room temperature for 16 h. Saturated aqueous sodium bicarbonate solution was added to quench the reaction. The mixture was extracted with EA. The combined organic solution was dried over anhydrous sodium sulphate. After filtration and concentration, the residue was purified by column chromatography to give 5-bromo-2-(2-methylpropyl)benzonitrile (D58) (36 g) as a colorless oil. 6H (CDCl3, 400 MHz): 0.96 (6H, d), 1.98 (1H, m), 2.69 (2H, d), 7.18 (1H, d), 7.64 (1H, dd), 7.55 (1H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389508B2
Source datasetuspto-grants-2013_03
ORD IDord-8b86e56db2c84ed3a0c9ac1afcf6695d
Source noteuspto-grants-2013_03