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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418147Generated: October 28, 2026

Diethyl Ether → 1-[3-Ethoxy-4-(trifluoromethyl)phenyl]ethanone

https://huagongshe.com/reaction/418147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
ReactantHCID 66650354HCID 66650354—
ReactantHCID 178418573HCID 178418573—
Catalystcopper(I) bromideHCID 24593—
Product1-[3-Ethoxy-4-(trifluoromethyl)phenyl]ethanoneHCID 6665033634%

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of 3-ethoxy-4-trifluoromethyl-benzonitrile from step 5 (5.00 g, 23.2 mmol), copper(I) bromide (100 mg, 0.7 mmol), tert.-butyldimethylchlorosilane (4.20 g, 27.9 mmol) in dry THF (30 mL) at −70° C. was drop wise added a 3 M methylmagnesium bromide solution in diethyl ether (13.2 mL, 39.6 mmol). The mixture was stirred at −70° C. for 10 min, then was warmed up to 0° C. and stirring was continued at 0° C. for further 2 h under nitrogen atmosphere. Poured the reaction mixture onto ice and sat. NH4Cl-sol., extracted three times with diethyl ether, washed the combined organic layers with brine, dried over MgSO4. Removal of the solvent in vacuum left a brown oil, which was purified by silica gel column chromatography with heptane/EtOAc 4:1 to give the title compound as a yellow liquid (1.84 g, 34%). MS (EI) 232 [M].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093263B2
Source datasetuspto-grants-2012_01
ORD IDord-8edfbd7ffe9544b4b36944cfa7743048
Source noteuspto-grants-2012_01