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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840062Generated: October 31, 2026

Water → 1-Bromo-6-methoxyhexane

https://huagongshe.com/reaction/840062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexaneHCID 8058—
Reactant1,6-DibromohexaneHCID 12368—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product1-Bromo-6-methoxyhexaneHCID 1303404393%

Reaction Steps

6-Bromohexyl methyl ether was prepared from 1,6-dibromohexane. To 48.8 g (200 mmol) of 1,6-dibromohexane at 60° C. was added 44 g (200 mmol) of a 25% solution of sodium methoxide in methanol. The reaction mixture was held 0.5 hours, then an additional 4 g of sodium methoxide solution was added, and the reaction mixture was held an additional hour. Hexane and water were added, the organic phase was washed with brine and dried with magnesium sulfate, filtered and stripped. Fractional distillation under vacuum gave 93% pure 6-bromohexyl methyl ether. This bromide was converted to the Grignard reagent, which was converted to 1-(7-methoxyheptyl)-cyclopropene in the same manner that pentylmagnesium bromide was converted to 1-hexylcyclopropene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06365549B2
Source datasetuspto-grants-2002_04
ORD IDord-01faa00a5ee743848313ef65f3dfd14c
Source noteuspto-grants-2002_04