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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914523Generated: October 26, 2026

1,2-Dimethoxyethane → 2-Chloro-4-(4-(trifluoromethyl)phenyl)pyrimidine

https://huagongshe.com/reaction/1914523

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2,4-DichloropyrimidineHCID 77531—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product2-Chloro-4-(4-(trifluoromethyl)phenyl)pyrimidineHCID 2186527672%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2,4-dichloro-pyrimidine (4.0 g, 27 mmol), 4-trifluoromethyl phenyl boronic acid (5.1 g, 27 mmol), tetrakis(triphenylphosphine)palladium(0) (1.5 g, 1.3 mmol), potassium phosphate (11 g, 54 mmol), 1,2-dimethoxyethane (50 mL) and water (10 mL) was heated to 80° C. under a blanket of nitrogen in a sealed tube. After 5 h, the mixture was partitioned between water (50 mL) and ethyl acetate (50 mL). The aqueous layer was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried (MgSO4), filtered, and concentrated. The residue was purified directly by FCC to afford a white solid (5.0 g, 72%). MS (ESI): mass calcd. for C11H6ClF3N2, 258.0; m/z found, 259.0 [M+H]+. 1H NMR (500 MHz, CDCl3) δ 8.74 (d, J=5.2, 1H), 8.23 (d, J=8.1, 2H), 7.80 (d, J=8.2, 2H), 7.71 (d, J=5.2, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614201B2
Source datasetuspto-grants-2013_12
ORD IDord-60588fd86e34447fb95f5c114d27a6b9
Source noteuspto-grants-2013_12