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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359324Generated: October 31, 2026

Ammonium Chloride → Ethyl 4-[3-(trifluoromethoxy)benzyl]benzoate

https://huagongshe.com/reaction/2359324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium ChlorideHCID 433294—
Reactant1-Bromo-3-(trifluoromethoxy)benzeneHCID 519964—
ReactantEthyl 4-(bromomethyl)benzoateHCID 954261—
ReactantSIPrHCID 10883669—
CatalystChlorotrimethylsilaneHCID 6397—
Catalyst1,2-DibromoethaneHCID 7839—
CatalystZincHCID 23994—
Catalyst1,3-Bis[2,6-di(propan-2-yl)phenyl]imidazolidin-2-ide;3-chloropyridine;dichloropalladiumHCID 58838879—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 4-[3-(trifluoromethoxy)benzyl]benzoateHCID 58046326101.7%

Reaction Steps

A mixture of zinc (807 mg, 12.3 mmol) and lithium chloride (523 mg, 12.3 mmol) under argon was warmed for 10 minutes using a hot air gun, allowed to cool and then anhydrous THF (50 mL) added. The zinc was activated by treatment with 1,2-dibromoethane (39 mg, 0.21 mmol) and TMSCl (4.3 mg, 0.04 mmol). To the resulting mixture at 25° C. was added ethyl 4-(bromomethyl)benzoate (1.0 g, 4.15 mmol) and the mixture stirred for 15 minutes. 3-(Trifluoromethoxy)bromobenzene (694 mg, 2.88 mmol) was added, followed by (1,3-bis(2,6-diisopropylphenyl)imidazolidene)(3-chloropyridyl)palladium(II) dichloride [PEPPSI™-SIPr] (28 mg, 0.04 mmol) and the mixture stirred at 25° C. for 1 hour. Saturated ammonium chloride solution was added and the crude product extracted with ether. The ether extract was washed with brine, dried over Na2SO4 and the solvent evaporated in vacuo. The crude product was purified by silica gel column chromatography eluting with 7:3 hexane:ethyl acetate to afford the title compound (950 mg, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685977B2
Source datasetuspto-grants-2014_04
ORD IDord-42f1bf1861394012932bf6d5969b32ba
Source noteuspto-grants-2014_04