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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297543Generated: October 30, 2026

1,3-Dimethoxybenzene → 1,3-Dimethoxy-2-(4-ethylbenzyl)benzene

https://huagongshe.com/reaction/1297543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DimethoxybenzeneHCID 9025—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(Bromomethyl)-4-ethylbenzeneHCID 12231560—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1,3-Dimethoxy-2-(4-ethylbenzyl)benzeneHCID 2307273249.7%

Reaction Steps

To a mixture of 1,3-dimethoxybenzene (6.9 g, 50 mmol) and tetrahydrofuran (70 mL), n-butyllithium (1.57 M in hexane, 35 mL) was added in ice and stirred for 1.5 hours. Subsequently, 4-ethylbenzyl bromide (10 g, 50 mmol) was added in ice and stirred for an additional 3.5 hours. After addition of saturated aqueous ammonium chloride, the reaction mixture was extracted with ethyl acetate, and the organic phase was washed with saturated aqueous sodium chloride and then dried over anhydrous magnesium sulfate. After the solvent was distilled off under reduced pressure, the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=95:5–85:15) to give 1,3-dimethoxy-2-(4-ethylbenzyl)benzene (6.37 g, 49%, mp 62.5–66.5° C.) as a light-yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250522B2
Source datasetuspto-grants-2007_07
ORD IDord-5e1f239e86fa409c985ddaa735520dc9
Source noteuspto-grants-2007_07