Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901818Generated: October 31, 2026

Azobisisobutyronitrile → HCID 11249951, compound

https://huagongshe.com/reaction/901818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantPerfluorodecyl iodideHCID 67920—
ReactantAllyltributylstannaneHCID 90628—
SolventHexaneHCID 8058—
ProductHCID 11249951HCID 1124995197%

Reaction Steps

In a typical procedure for reverse fluorous solid phase extraction in the studies of FIG. 4, a perfluoroalkyl iodide such as perfluorodecyl iodide (RfI, 323 mg, 0.5 mmol), allyltributyltin (330 mg, 1 mmol), AIBN (9 mg, 0.05 mmol) and hexane (5 ml) were placed in a flask under an argon atmosphere and the mixture was refluxed for 5 h. After removal of the volatile components by evaporation, the mixture was submitted to separation by reverse fluorous solid phase extraction. A short column was packed with regular silica gel (6.0 g) using FC-72/Et2O (2/1) as the solvent. The crude reaction mixture was then loaded onto this column and eluted with 20 ml of FC-72/Et2O (2/1) to give 3-(perfluorodecyl)prop-1-ene in 97% yield (271 mg). After similar reactions and separations, the allylated products 2a-d, 3a-d and 4a-d were isolated in yields ranging from 69-93%. The nuclear magnetic resonance (NMR) spectra of these products were clean, and gas chromatography (GC) or high pressure liquid chromatography (HPLC) purities exceeded 90% in all cases. The purity of the products was determined by GC in the case of R═H or R═Me and HPLC (Nova Pak® Silica, UV detection at 254 nm) in the case of R═Ph.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07364908B2
Source datasetuspto-grants-2008_04
ORD IDord-62ecb49063c34ababe95f7a6e41f56b0
Source noteuspto-grants-2008_04