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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904975Generated: October 26, 2026

Sodium hydride → 2-(4-Ethoxyphenyl)-3,3,3-trifluoropropyl 3-(4-bromophenoxy)benzyl ether

https://huagongshe.com/reaction/1904975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(RS)-1,1,1-trifluoro-2-(4-ethoxyphenyl)propan-3-olHCID 10681171—
Reactant3-(4-Bromophenoxy)benzyl bromideHCID 14517055—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Ethoxyphenyl)-3,3,3-trifluoropropyl 3-(4-bromophenoxy)benzyl etherHCID 1405398930.8%

Reaction Steps

Under a nitrogen atmosphere, 171 mg of sodium hydride (60% oil dispersion) was added to 20 ml of dry THF. A solution of 1.0 g of 2-(4-ethoxyphenyl)-3,3,3-trifluoropropanol and 1.30 g of 3-(4-bromophenoxy)benzyl bromide in 30 ml of dry THF was then added with ice-cooling, and the reaction solution was stirred with ice-cooling for 1 hour and at room temperature for 12 hours. Thereafter, the reaction mixture was poured into dilute HCl-ice water and extracted twice with diethyl ether. The ether layers were combined, washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed under a reduced pressure, and the residue was subjected to column chromatography on silica gel [eluted with n-hexane/ethyl acetate (50:1) mixture] to obtain 0.58 g of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04840971
Source datasetuspto-grants-1989_06
ORD IDord-281aa55ea39d473b916f0d69f32271fe
Source noteuspto-grants-1989_06