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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728546Generated: October 26, 2026

Myristyl bromide → 3-(Tetradecyloxy)benzenemethanol

https://huagongshe.com/reaction/1728546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMyristyl bromideHCID 8208—
ReactantSodium HydroxideHCID 14798—
Reactant3-Hydroxyphenethyl alcoholHCID 83404—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventTolueneHCID 1140—
Product3-(Tetradecyloxy)benzenemethanolHCID 10041710652.2%

Reaction Steps

A mixture of 66 g of 3-hydroxyphenethyl alcohol, 147.43 g of 1-bromotetradecane, 27.65 g of sodium hydroxide and 2.15 g of trioctylmethyl ammonium chloride in 400 ml of toluene was refluxed for 42 hours. The mixture was washed with water and the organic layer dried with magnesium sulfate. The solvent was removed in vacuo and the warm concentrate poured into 1 liter of hexanes. The resulting solid was washed with cold hexanes then dried giving 998.6 g of the desired compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05328901
Source datasetuspto-grants-1994_07
ORD IDord-1f9b5896a10c465a869b7a9104213deb
Source noteuspto-grants-1994_07