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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614449Generated: November 1, 2026

Sodium Hydroxide → 2-(4-Ethoxyphenyl)-3,3,3-trifluoropropyl 3-phenoxybenzyl ether

https://huagongshe.com/reaction/1614449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1-(Bromomethyl)-3-phenoxybenzeneHCID 94544—
Reactant(RS)-1,1,1-trifluoro-2-(4-ethoxyphenyl)propan-3-olHCID 10681171—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
Product2-(4-Ethoxyphenyl)-3,3,3-trifluoropropyl 3-phenoxybenzyl etherHCID 1066958129.5%

Reaction Steps

A mixture of 1,1,1-trifluoro-2-(4-ethoxyphenyl)propan-3-ol (0.4 g), 3-phenoxybenzyl bromide (0.45 g), tetra-n-butylammonium hydrogen sulphate (0.05 g) and aqueous sodium hydroxide solution (40% w/v, 5.0 cm3) was stirred at the ambient temperature for 6 hours after which it was partitioned between water and diethyl ether. The ethereal phase was separated, washed twice with water, dried over anhydrous magnesium sulphate and concentrated by evaporation of the solvent under reduced pressure. The residual oil (0.75 g) was purified by chromatography on a silica gel column eluted with a mixture of hexane (23 parts by volume) and ethyl acetate (2 parts by volume) to yield 1,1,1-trifluoro-2-(4-ethoxyphenyl)-3-(3-phenoxybenzyloxy) propane (0.21 g) as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05196610
Source datasetuspto-grants-1993_03
ORD IDord-43c4b4050ebe4f45a5482e5ec3554940
Source noteuspto-grants-1993_03