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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099035Generated: October 25, 2026

Sodium Iodide → 1-Bromo-4-(1-methyl-hexyloxy)-benzene

https://huagongshe.com/reaction/2099035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant4-BromophenolHCID 7808—
ReactantPotassium CarbonateHCID 11430—
Reactant2-BromoheptaneHCID 16090—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
Product1-Bromo-4-(1-methyl-hexyloxy)-benzeneHCID 2009678560.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

p-Bromophenol (295.52 grams (“g”), 1500.00 millimole) is dissolved in anhydrous dimethyl formamide (“DMF”) (500 milliliters) in a 2000 milliliter (“mL”) 3-necked flask equipped with mechanical stirrer and condenser, under an argon atmosphere. To this solution, (1-methyl)hexylbromide (322.38 grams, 1800.00 millimoles), sodium iodide (33.57 g, 225.00 mmol) and anhydrous potassium carbonate (621.95 g, 4500.00 mmol) are added. The resulting suspension is heated to 100° C. and stirred at that temperature for 72 hours. After cooling to room temperature, water (1000 mL) and n-hexane (300 mL) are added. The aqueous layer is separated and extracted with n-hexane (3×100 mL). The combined organic layers are washed with diluted sodium chloride solution (2×100 mL) and dried (MgSO4). The solvent is removed by rotary evaporation under reduced pressure and the residue is filtered using a SiO2 layer (10×10 cm) and n-hexane as eluent. After removal of solvent by rotary evaporation and in vacuo a colorless liquid (245.54 g, 60%) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569415B2
Source datasetuspto-grants-2009_08
ORD IDord-d5c2aaa7d3d64341b08fcb6fcbab8a7f
Source noteuspto-grants-2009_08