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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816726Generated: October 25, 2026

Sodium Methoxide → 5-Bromo-2-(7-methoxyheptyloxy)-1,3-dimethylbenzene

https://huagongshe.com/reaction/1816726

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant5-Bromo-2-(7-bromoheptyloxy)-1,3-dimethylbenzeneHCID 22494636—
SolventMethanolHCID 887—
Product5-Bromo-2-(7-methoxyheptyloxy)-1,3-dimethylbenzeneHCID 22494771—

Reaction Steps

A solution of crude 5-bromo-2-(7-bromoheptyloxy)-1,3-dimethylbenzene (7.81 g) in methanol (78 ml) was treated with 28% sodium methoxide in methanol (78 ml), and the solution was refluxed for 8 hours. After cooling, the reaction mixture was evaporated under reduced pressure, and the residue was extracted with methylene chloride. The organic layer was dried over magnesium sulfate and magnesium sulfate was filtered off, and then the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography eluting with a mixed solvent of n-hexane-ethyl acetate (from 0% to 7% gradient elution) to give 5-bromo-2-(7-methoxyheptyloxy)-1,3-dimethylbenzene (3.34 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884868B1
Source datasetuspto-grants-2005_04
ORD IDord-f2cfa733b5be49458a48c3a789d932ac
Source noteuspto-grants-2005_04