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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843773Generated: November 1, 2026

4-Ethylphenol → HCID 58442373, compound

https://huagongshe.com/reaction/1843773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-EthylphenolHCID 31242—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-(4-chloro-2,6-dimethylphenyl)ethanoneHCID 53402864—
Catalystpalladium(II) acetateHCID 167845—
CatalystDi-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
SolventTolueneHCID 1140—
ProductHCID 58442373HCID 5844237382%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 1-(4-chloro-2,6-dimethylphenyl)ethanone (5.0 g, 27.4 mmol), K3PO4 (11.6 g, 54.7 mmol), 4-ethylphenol (4.01 g, 32.8 mmol) in toluene (54.8 mL) was added 2-di-tert-butylphosphino-2′,4′,6′-triisopropylbiphenyl (349 mg, 0.82 mmol) and Pd(OAc)2 (259 mg, 1.15 mmol). The reaction was heated at 100° C. overnight under N2. The solution was cooled to room temperature and filtered through a small pad of Celite. The cake was washed with ethyl acetate (50 mL) and combined filtrate was concentrated under reduced pressure. The residue was purified by flash column chromatography on silica gel to give 1-(4-(4-ethylphenoxy)-2,6-dimethylphenyl)ethanone (6.0 g) as yellow oil in 82% yield: 1H NMR (500 MHz, CDCl3) δ 7.17 (d, J=8.5 Hz, 2 H), 6.93 (d, J=8.5 Hz, 2 H), 6.63 (s, 2 H), 2.64 (q, J=7.5 Hz, 2 H), 2.47 (s, 3 H), 2.21 (s, 6 H), 1.25 (t, J=7.5 Hz, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946268B2
Source datasetuspto-grants-2015_02
ORD IDord-1dfcdd4cf43f436c9227158d5170f196
Source noteuspto-grants-2015_02