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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465637Generated: October 29, 2026

4-Ethylphenol → HCID 58442373, compound

https://huagongshe.com/reaction/1465637

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 diatomaceous earth. 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, 2H), 2.64 (q, J=7.5 Hz, 2 H), 2.47 (s, 3 H), 2.21 (s, 6 H), 1.25 (t, J=75 Hz, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999983B2
Source datasetuspto-grants-2015_04
ORD IDord-c9a5fca3172a46ef916dd24f081bf774
Source noteuspto-grants-2015_04