HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261012Generated: October 30, 2026
Azobisisobutyronitrile → Phosphine, octyl-
https://huagongshe.com/reaction/261012
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | 1-Octene | HCID 8125 | — |
| Reactant | Phosphine | HCID 24404 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Phosphine, octyl- | HCID 446269 | 70% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04163760 |
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| Source dataset | uspto-grants-1979_08 |
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| ORD ID | ord-d4864d5bbe6f48d9941e79dc4c7f0d38 |
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| Source note | uspto-grants-1979_08 |
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