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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612601Generated: October 30, 2026

Isopropyl iodide → 1-Bromo-2-(1-methylethoxy)benzene

https://huagongshe.com/reaction/612601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl iodideHCID 6362—
Reactant2-BromophenolHCID 7244—
ReactantPotassium CarbonateHCID 11430—
SolventIsopropanolHCID 3776—
Product1-Bromo-2-(1-methylethoxy)benzeneHCID 21925427—

Reaction Steps

Prepare a stirred mixture of ortho-bromo-phenol (25.951 g, 17.4 mL, 0.15 mole) and potassium carbonate (20.70 g, 0.16 mole) in 175 mL isopropanol at ambient temperature under argon. Slowly add isopropyl iodide (22.2 g, 16.00 mL), heat at reflux and stir the mixture overnight. Cool to ambient temperature then filter, condensing the filtrate on a rotary evaporator. Dissolve the residual oil in diethyl ether (300 mL) and twice extract with 100 mL 50% sodium hyroxide. Separate, wash with brine and concentrate on a rotary evaporator to give a pale yellow liquid. Distill on the Kugelrohr (0.05 mm, 100°-120° C.) to obtain the title compound as an oil. (24.21 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06004959
Source datasetuspto-grants-1999_12
ORD IDord-b757932acdd7444b92733299de2b5f67
Source noteuspto-grants-1999_12