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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178671Generated: October 29, 2026

2-Bromophenol → 1-bromo-2-(2-bromoethoxy)benzene

https://huagongshe.com/reaction/2178671

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromophenolHCID 7244—
Reactant1,2-DibromoethaneHCID 7839—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product1-bromo-2-(2-bromoethoxy)benzeneHCID 2734928—

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 2-bromophenol (3.50 g, 20.23 mmol), 1,2-dibromoethane (19.00 g, 101 mmol), and potassium carbonate (7.06 g, 2.92 mmol) in acetonitrile (50 mL) was heated to 80° C. After heating overnight, the reaction mixture was cooled to room temperature, diluted with ethyl acetate and washed with water and saturated aqueous sodium chloride solution. The organic layer was dried over magnesium sulfate, filtered and the filtrate was concentrated in vacuo to afford the title compound as a clear oil. Yield: 6.36 g, 100%. 1H NMR (400 MHz, CDCl3) δ 3.69 (dd, J=6.6, 6.4 Hz, 2H), 4.35 (dd, J=6.7, 6.4 Hz, 2H), 6.87-6.94 (m, 2H), 7.25-7.30 (m, 1H), 7.56 (dd, J=7.9, 1.6 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067934B2
Source datasetuspto-grants-2015_06
ORD IDord-1e2ee62ebde04d58ab5b06f5a8e34e97
Source noteuspto-grants-2015_06