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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843764Generated: November 1, 2026

3,5-Dimethylphenol → HCID 58442376, compound

https://huagongshe.com/reaction/1843764

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-DimethylphenolHCID 7948—
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 58442376HCID 5844237686%

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), 3,5-dimethylphenol (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), 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-(3,5-dimethylphenoxy)-2,6-dimethylphenyl)ethanone (6.3 g) as yellow solids in 86% yield: 1H NMR (500 MHz, CDCl3) δ 6.76 (s, 1 H), 6.63 (s, 2 H), 6.62 (s, 2 H), 2.48 (s, 3 H), 2.29 (s, 6 H), 2.22 (s, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946268B2
Source datasetuspto-grants-2015_02
ORD IDord-c7bd6855d80d4f99b65e0ba528f0c8af
Source noteuspto-grants-2015_02