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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617454Generated: November 4, 2026

Triphenylphosphine → HCID 136166843, compound

https://huagongshe.com/reaction/1617454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantAmmonium ChlorideHCID 25517—
ReactantPotassium FluorideHCID 522689—
Reactant(Pyrimidin-5-yl)boronic acidHCID 2795193—
ReactantHCID 136167080HCID 136167080—
CatalystHCID 178418397HCID 178418397—
SolventN,N-Dimethylacetamide--water (1/1)HCID 21534740—
ProductHCID 136166843HCID 136166843451%

Reaction Steps

To a stirred solution of (E)-3-(4-bromo-phenyl)-3-phenyl-1-pyridin-4-yl-propan-1-one oxime (example 5, 10 mg) and pyrimidine-5-boronic acid (49 mg) in a mixture of DMA/H2O (2.1 mL, 20:1) tetrakis(triphenylphosphine)palladium (0) (36 mg), triphenylphosphine (17 mg) and potassium fluoride (31 mg) were added. The mixture was irradiated in the microwave at 140° C. for 15 min. A saturated aqueous solution of NH4Cl was added, the phases were separated and the inorganic one was extracted with EtOAc (2×). The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The crude product was purified by flash chromatography on an ISOLUTE Flash NH2 cartridge (EtOAc) to yield the title compound (45 mg, 45%) as a white foam, MS (ESI+): m/z=381.1 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765730B2
Source datasetuspto-grants-2014_07
ORD IDord-8723b02b9efa436390a89b4f5debc9fb
Source noteuspto-grants-2014_07