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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585339Generated: October 25, 2026

Bromine → 1-Bromo-2,4-bis(methoxymethyl)benzene

https://huagongshe.com/reaction/585339

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium SulfiteHCID 24437—
ReactantSodium AcetateHCID 517045—
Reactant1,3-Bis(methoxymethyl)benzeneHCID 6430775—
SolventAcetic AcidHCID 176—
Product1-Bromo-2,4-bis(methoxymethyl)benzeneHCID 1296888529.7%

Reaction Steps

To a solution of m-xylylene dichloride (25.0 g) in methanol (125 ml) was added a 28% methanol solution (82.6 g) containing sodium methoxide at room temperature, and the mixture was stirred with heating at 60° C. for 3 hr. The solvent was evaporated and water (150 ml) was added to the residue. The mixture was extracted twice with heptane (80 ml) and heptane was evaporated under reduced pressure to give m-xylylene glycol dimethyl ether (25.3 g). m-Xylylene glycol dimethyl ether (25.3 g) was dissolved in acetic acid (125 ml) and sodium acetate (68 g) was added, which was followed by dropwise addition of bromine (68 g) at room temperature. The mixture was stirred at room temperature for 3 hr and poured into 10% aqueous sodium sulfite solution (750 ml), which mixture was extracted twice with heptane (350 ml). The heptane layer was extracted twice with 10% aqueous sodium hydroxide solution (150 ml) and once with water (150 ml). The solvent was evaporated and the residue was purified by silica gel column chromatography using heptane-ethyl acetate (15:1) as an eluent to give the title compound (10.4 g, yield: 29.7%) as a colorless transparent oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06930211B2
Source datasetuspto-grants-2005_08
ORD IDord-23c06944566441d9b29e35f7a2b11f17
Source noteuspto-grants-2005_08