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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422053Generated: October 31, 2026

2-Bromophenol → 1-Bromo-2-(3-methylbutoxy)benzene

https://huagongshe.com/reaction/422053

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromophenolHCID 7244—
Reactant1-Bromo-3-methylbutaneHCID 7891—
ReactantPotassium CarbonateHCID 11430—
SolventAcetonitrileHCID 6342—
Product1-Bromo-2-(3-methylbutoxy)benzeneHCID 2836954693%

Reaction Conditions

Temperature80 °C

Reaction Steps

A 500 mL of round-bottom flask was charged with 2-bromophenol (43 g, 0.25 mol), 1-bromo-3-methylbutane (41 mL, 0.325 mol), acetonitrile (200 mL) and potassium carbonate (52 g). The reaction mixture was heated to 80° C. with stirring overnight. The reaction was cooled and filtered, and washed with acetonitrile. The filtrate was concentrated in vacuo. Vacuum distillation of the residue yielded 1-bromo-2-(isopentyloxy)benzene (83-86° C., 56 g, 93% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101625B2
Source datasetuspto-grants-2012_01
ORD IDord-1bafd11df4aa43b08ce8aa61bc6cf586
Source noteuspto-grants-2012_01