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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159060Generated: November 5, 2026

Potassium Acetate → N,N-diethyl-4-hydroxy-2-(trifluoromethoxy)benzamide

https://huagongshe.com/reaction/1159060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium AcetateHCID 517044—
ReactantBis(pinacolato)diboraneHCID 2733548—
Reactant4-bromo-N,N-diethyl-2-(trifluoromethoxy)benzamideHCID 68687835—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductN,N-diethyl-4-hydroxy-2-(trifluoromethoxy)benzamideHCID 6868719882.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirring degassed solution of N,N-diethyl-4-bromo-2-(trifluoromethoxy)benzamide (2768 mg, 8.2 mmol), bis(pinacolato)diboron (2281 mg, 9.0 mmol), and potassium acetate (2402 mg, 24.5 mmol) in dry DMF (60 mL) was added palladium(II) acetate (55 mg, 0.25 mmol). The reaction was heated to 80° C. for 2 h and then cooled to room temp. The reaction was quenched with water and extracted with EtOAc (3×75 mL). The organic layers were combined, dried over Na2SO4, and conc. in vacuo to a brown oil. The oil was dissolved in THF (40 mL) and acetic acid (2.0 mL) and treated with hydrogen peroxide (8 mL). The reaction was stirred for 15 min and then quenched with st. aq. NaHSO3. The reaction was extracted with EtOAc (3×40 mL). The organic layers were combined, dried over Na2SO4, and conc. in vacuo to a brown oil. The oil was purified by flash chromatography (silica gel, 20-70% EtOAc in hexanes) to give 1876 mg of the desired product as a white solid. MS (ESI) 278 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812024B2
Source datasetuspto-grants-2010_10
ORD IDord-a2281878d97d4255bc70dab15c0f2a72
Source noteuspto-grants-2010_10