Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965872Generated: October 30, 2026

Triphenylphosphine → HCID 11816425, compound

https://huagongshe.com/reaction/965872

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-Chloro-5-nitropyridineHCID 78308—
ReactantHCID 4372073HCID 4372073—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductHCID 11816425HCID 1181642523%

Reaction Steps

Under inert atmosphere (Ar) a mixture of palladium(II)-acetate (0.45 g , 2 mmol) and triphenylphosphine (0.95 g, 3.6 mmol) in DMF (50 ml) was stirred for 0.5 hr at rt. Then 2-chloro-5-nitropyridine (3.2 g, 20 mmol) and tributyl-styryl-stannane (15.7 g, 40 mmol) was added and the mixture was stirred at 130° C. for 15 hr. The solvent was evaporated and the residue partitioned between AcOEt and 1N HCl. The aqueous phase was neutralized with 6N NaOH and extracted with AcOEt. The organic phase was dried with Na2SO4, concentrated and chromatographed (SiO2 with CH2Cl2/CH3OH=97/3) to (give the title compound (0.90 g, 23%) as a yellow solid. Mp. 159-160° C. (AcOEt), MS: 196 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951875B2
Source datasetuspto-grants-2005_10
ORD IDord-4490c8e23c9f4de9b204d6a236698d5b
Source noteuspto-grants-2005_10