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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366569Generated: October 31, 2026

1,4-Dibromobutane → 1-(4-BROMOPHENYL)CYCLOPENTANECARBONITRILE

https://huagongshe.com/reaction/2366569

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantBenzeneacetonitrile, 4-bromo-HCID 27914—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTetrahydrofuranHCID 8028—
Product1-(4-BROMOPHENYL)CYCLOPENTANECARBONITRILEHCID 3987679—

Reaction Steps

To a solution of 2-(4-bromophenyl)acetonitrile (1.0 g, 5.10 tntnol) and 1,4-dibromobutane (0.67 ml, 5.6 mmol) in THF (10 ml) was added potassium bis(trimethylsilyl) amide (2.23 g, 11.2 mmol) and tetra-n-butylammonium bromide (164 mg, 0.51 mmol). The mixture was stirred for 2 h and then quenched with 1N HCl. Ethyl acetate was added, the layers separated and the organic layer was washed with water and brine. Drying, solvent evaporation and flash chromatography (silica gel, 20% EtOAc/hexanes) gave 1-(4-bromophenyl)cyclopentanecarbonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697863B2
Source datasetuspto-grants-2014_04
ORD IDord-903a9014c1bb4be8a7eabac0fc306023
Source noteuspto-grants-2014_04