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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843770Generated: November 2, 2026

1-Chloro-4-(trifluoromethyl)benzene → HCID 67387269, compound

https://huagongshe.com/reaction/1843770

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(trifluoromethyl)benzeneHCID 7394—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-(4-Hydroxy-2,6-dimethylphenyl)ethanoneHCID 4057370—
ReactantDi-tert-butyl(2',4',6'-tris(propan-2-yl)-(1,1'-biphenyl)-2-yl)phosphaneHCID 11618717—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductHCID 67387269HCID 6738726919.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 1-chloro-4-(trifluoromethyl)benzene (6.60 g, 36.6 mmol), K3PO4 (12.9 g, 60.9 mmol), 1-(4-hydroxy-2,6-dimethylphenyl)ethanone (5.00 g, 30.5 mmol) in toluene (60.9 mL) was added 2-di-tert-butylphosphino-2′,4′,6′-triisopropylbiphenyl (388 mg, 0.91 mmol) and Pd(OAc)2 (288 mg, 1.28 mmol). The reaction was heated at 100° C. for 120 min 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-(2,6-dimethyl-4-(4-(trifluoromethyl)phenoxy)phenyl)ethanone (1.8 g) as yellow oil in 19% yield: 1H NMR (500 MHz, CDCl3) δ 7.58 (d, J=8.5 Hz, 2 H), 7.04 (d, J=8.5 Hz, 2 H), 6.70 (s, 2 H), 2.50 (s, 3 H), 2.25 (s, 6 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946268B2
Source datasetuspto-grants-2015_02
ORD IDord-a376ac6ca971498289b14e5847c5ebbb
Source noteuspto-grants-2015_02