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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57395Generated: October 26, 2026

Potassium Phosphate, Tribasic → 1-(5-(3-(Trifluoromethyl)phenyl)pyrimidin-2-yl)ethanone

https://huagongshe.com/reaction/57395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
Reactant1-(5-Bromopyrimidin-2-yl)ethan-1-oneHCID 53488064—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product1-(5-(3-(Trifluoromethyl)phenyl)pyrimidin-2-yl)ethanoneHCID 8673017265.5%

Reaction Steps

A cloudy solution of 1-(5-bromopyrimidin-2-yl)ethanone (300 mg, 1.49 mmol), 3-(trifluoromethyl)phenylboronic acid (567 mg, 2.98 mmol), K3PO4 (950 mg, 4.48 mmol), DavePhos ligand [2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl](59 mg, 0.15 mmol), and Pd(OAc)2 (17 mg, 0.075 mmol) in 6 mL toluene was heated at 100° C. for 1 h. The mixture was cooled to room temperature, and filtered through Celite. Filter cake was rinsed with 30 mL EtOAc. The filtrate was poured into 20 mL water. Layers were separated, and the aqueous was further extracted with EtOAc (20 mL). Combined organics were washed with water (20 mL) and brine (20 mL), dried over Na2SO4, filtered and concentrated directly onto silica gel. Column chromatography (10-100% EtOAc/heptane) gave 0.26 g 1-(5-(3-(trifluoromethyl)phenyl)pyrimidin-2-yl)ethanone as tan solid. MS m/z 267.1 (M+H)+. 1H NMR (400 MHz, CDCl3) δ 9.16 (s, 2H), 7.93-7.69 (m, 4H), 2.87 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434719B2
Source datasetuspto-grants-2016_09
ORD IDord-1308a2f6995e48148fcbb0c8db6844bd
Source noteuspto-grants-2016_09