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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067882Generated: October 27, 2026

Potassium Carbonate → 2-Chloro-5-(4-(difluoromethoxy)phenyl)pyrimidine

https://huagongshe.com/reaction/2067882

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
Reactant2-(4-(Difluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 22032303—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Product2-Chloro-5-(4-(difluoromethoxy)phenyl)pyrimidineHCID 58171930—

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 5-bromo-2-chloropyrimidine 4 (7.7 mmol) in 1,4-dioxane (1.5 mL) is added 2-(4-(difluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 7 (8.9 mmol), 1.8M K2CO3 aq. (16.2 mmol) and Pd(PPh3)4 (0.38 mmol). The reaction is evacuated and backfilled with nitrogen twice then heated at 150° C. for 10 min under microwave. After this time, the reaction mixture is diluted with a saturated solution of NH4Cl and extracted with DCM (3×50 mL). The organic layer is washed with brine, dried over Na2SO4 and concentrated. Purification by short silica gel chromatography using a hexane:EtOAc=3:1 mixture affords 2-chloro-5-(4-(difluoromethoxy)phenyl)pyrimidine 30. 1HNMR (400 MHz, CDCl3) δ 8.73 (s, 2H), 7.47-7.52 (m, 2H), 7.20-7.24 (m, 2H), 6.52 (t, J=72 Hz, 1H). MS (m/z) (M+1)+: 257.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293757B2
Source datasetuspto-grants-2012_10
ORD IDord-84af6fd6e3034739b31d6e2963cf6dad
Source noteuspto-grants-2012_10