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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54025Generated: October 26, 2026

Hexane → 2-Bromo-1,3-dimethoxybenzene

https://huagongshe.com/reaction/54025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
Reactant1,3-DimethoxybenzeneHCID 9025—
ReactantCarbon tetrabromideHCID 11205—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product2-Bromo-1,3-dimethoxybenzeneHCID 61229657.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a solution of 1,3-dimethoxybenzene (3.0 g, 21.7 mmol) dissolved in diethyl ether (90 ml), a 1.65M solution of n-butyl lithium in n-hexane (19.8 ml, 32.7 mmol of n-butyl lithium) was added at room temperature, and a reaction mixture was heated to reflux for 4 hours. After cooling the reaction mixture to 0° C., a solution of carbon tetrabromide (15.8 g, 47.7 mmol) in diethyl ether (60 ml) was added to the mixture, and stirred at room temperature for 20 hours. A small amount of water was added to the reaction mixture, and then the reaction mixture was diluted with ethyl acetate (90 ml). The organic layer was washed with water and dried over anhydrous magnesium sulfate. Thereafter, the solvent was evaporated off, and the residue was purified by column chromatography to obtain 1-bromo-2,6-dimethoxybenzene (2.70 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05621129
Source datasetuspto-grants-1997_04
ORD IDord-fc9b38681b0e43a0aaebc84a04652613
Source noteuspto-grants-1997_04