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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410319Generated: October 25, 2026

Potassium Phosphate, Tribasic → 4-chloro-5-(3,6-dihydro-2H-pyran-4-yl)pyrimidine

https://huagongshe.com/reaction/410319

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3,6-Dihydro-2H-pyran-4-boronic acid pinacol esterHCID 11218053—
Reactant4-Chloro-5-iodopyrimidineHCID 11230204—
Catalystpalladium(II) acetateHCID 167845—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product4-chloro-5-(3,6-dihydro-2H-pyran-4-yl)pyrimidineHCID 59326832—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 150 mL sealable flask was added potassium phosphate (4.21 g, 19.83 mmol), dppf (0.264 g, 0.476 mmol), diacetoxypalladium (0.053 g, 0.238 mmol), 4-chloro-5-iodopyrimidine (1.907 g, 7.93 mmol), and 2-(3,6-dihydro-2H-pyran-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.75 g, 8.33 mmol) as a solution in DME (45.3 mL)/water (7.56 mL). The vessel was sealed and heated to 80° C. for 20 h. The reaction mixture was cooled to room temperature and diluted with water before extracting with ethyl acetate. The combined organics were dried over sodium sulfate, filtered, and concentrated under reduced pressure to a dark brown oil that was used without purification. MS (ESI, pos. ion) m/z: 176.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759532B2
Source datasetuspto-grants-2014_06
ORD IDord-ddac7db3e3b54dd7b8bbbe0e84b6c957
Source noteuspto-grants-2014_06