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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773048Generated: November 2, 2026

Cesium carbonate → 4-Chloro-6-phenylpyrimidine

https://huagongshe.com/reaction/1773048

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantPhenylboronic AcidHCID 66827—
Reactant4,6-DichloropyrimidineHCID 70943—
ReactantTricyclohexylphosphineHCID 75806—
Solvent1,4-DioxaneHCID 31275—
Product4-Chloro-6-phenylpyrimidineHCID 59342934%

Reaction Steps

First, into a recovery flask equipped with a reflux pipe were put 3.35 g of 4,6-dichloropyrimidine, 3.02 g of phenylboronic acid, 1.7 mL of tricyclohexylphosphine (abbreviation: Cy3P), 14.7 g of cesium carbonate, 0.31 g of tris(dibenzylideneacetone)palladium(0) (abbreviation: Pd2(dba)3), and 30 mL of dioxane, and the air in the flask was replaced with argon. This reaction container was heated by irradiation with microwaves (2.45 GHz, 120 W) for 60 minutes for reaction. The solvent of this solution was distilled off, and then the obtained residue was purified by silica gel column chromatography using a mixed solvent of dichloromethane and hexane as a developing solvent in a volume ratio of 1:1, to give 4-chloro-6-phenylpyrimidine (light yellow powder, 34% in yield). Note that the irradiation with microwaves was performed using a microwave synthesis system (Discover, manufactured by CEM Corporation). A synthesis scheme of Step 1 is shown in (b-1) given below.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09252380B2
Source datasetuspto-grants-2016_02
ORD IDord-f97594e447ff494cbe8da9c08f9cb656
Source noteuspto-grants-2016_02