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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710395Generated: November 2, 2026

Triphenylphosphine → HCID 178454879, compound

https://huagongshe.com/reaction/1710395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 178478446HCID 178478446—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHCID 178454879HCID 178454879—

Reaction Conditions

Temperature90 °C

Reaction Steps

4.0 g of 6-bromo-2-chloromethyl-3H-imidazo[4,5-b]pyridine (compound J1) are suspended in 16 ml of N,N-dimethylformamide and 54 ml of acetonitrile. 4.9 ml of triphenylphosphine and 0.599 g of tetrabutylammonium iodide are added sequentially at 40° C. and the mixture is heated to 90° C. for 20 h. The mixture is concentrated to dryness to give the 8.94 g of the crude title compound as an oil, which is used as obtained. MS: 412.3, 414.2 (M+). TLC: Rf=0.40-0.55 (dichloromethane/methanol 10:1 parts by volume).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790710B2
Source datasetuspto-grants-2010_09
ORD IDord-6cbd74b4d35d43e08dfa717f6b3d79a3
Source noteuspto-grants-2010_09