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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261012Generated: October 30, 2026

Azobisisobutyronitrile → Phosphine, octyl-

https://huagongshe.com/reaction/261012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
Reactant1-OcteneHCID 8125—
ReactantPhosphineHCID 24404—
SolventBenzeneHCID 241—
ProductPhosphine, octyl-HCID 44626970%

Reaction Conditions

Temperature90 °C

Reaction Steps

A 1-liter autoclave was charged with 5 g of azobisisobutyronitrile, 50 g of benzene and 112 g (1 mol) of 1-octene, and 136 g (4 mols) of hydrogen phosphide was condensed thereinto. The whole was heated to 90° C. The pressure initially rose to 70 bars, then dropped gradually to 55 bars, and remained constant after 5 hours. The reaction mixture was analyzed by NMR-spectroscopy. The octene conversion rate was 85%. Primary octylphosphine was obtained in a yield of 70%, secondary octylphosphine was obtained in a yield of 20%, and tertiary octylphosphine was obtained in a yield at 10%, based on the quantity of 1-octene which underwent conversion.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04163760
Source datasetuspto-grants-1979_08
ORD IDord-d4864d5bbe6f48d9941e79dc4c7f0d38
Source noteuspto-grants-1979_08