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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546948Generated: October 27, 2026

Potassium Phosphate, Tribasic → HCID 57454141, compound

https://huagongshe.com/reaction/546948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantEthyl 2-(2-bromopyrimidin-5-yl)acetateHCID 57443494—
ReactantHCID 57709023HCID 57709023—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductHCID 57454141HCID 5745414141%

Reaction Conditions

Temperature95.5 °C

Reaction Steps

Degassed N,N-dimethylformamide (0.32 mL) was added to 2-[4-(1-{4-[(E)-3-(t-butyl-dimethyl-silanyloxy)-4,4,4-trifluoro-3-trifluoromethyl-1-butenyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (Example 77-(1); 35.8 mg, 0.0523 mmol), 2-bromopyrimidine-5-acetic acid ethyl ester (Example 43-(3); 37.3 mg, 0.152 mmol), tetrakis(triphenylphosphine)palladium (0) (29.8 mg, 0.0258 mmol) and potassium phosphate (48.7 mg, 0.229 mmol). After replacement with nitrogen, the mixture was heated while stirring at an external temperature of 91 to 100° C. for 10 hours. Water was added to the reaction mixture, followed by extraction with diethyl ether. The extract was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel chromatography (hexane/ethyl acetate=4/1) to give the title compound (13 mg, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935688B2
Source datasetuspto-grants-2011_05
ORD IDord-610b11214dc440febaf0223b2a15078a
Source noteuspto-grants-2011_05