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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471836Generated: October 30, 2026

4-Bromophenol → 2-(4-bromophenoxy)acetonitrile

https://huagongshe.com/reaction/471836

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromophenolHCID 7808—
ReactantCesium carbonateHCID 10796—
ReactantBromoacetonitrileHCID 11534—
SolventAcetonitrileHCID 6342—
Product2-(4-bromophenoxy)acetonitrileHCID 598823—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of p-bromophenol (2.61 g; 15.1 mmol), bromoacetonitrile (1.11 mL; 15.9 mmol), and Cs2CO3 (7.40 g; 22.7 mmol) in anhyd MeCN (25 mL) was heated at 80° C., under N2 overnight. The mixture was cooled, filtered through a pad of Celite and concentrated in vacuo. The residue was dissolved in a minimal amount of EtOAc/hexanes and filtered through a short pad of silica gel (EtOAc/hexanes eluent), affording the title compound as a colorless, waxy solid which was used without further purification. 1H NMR (400 MHz, CDCl3) δ 4.75 (s, 2H), 6.88 (m, 2H), 7.46 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633175B2
Source datasetuspto-grants-2014_01
ORD IDord-168c5344756b4f5081c752a787278b66
Source noteuspto-grants-2014_01