HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420831Generated: October 25, 2026
Azobisisobutyronitrile → 9-Cyclopentyl-9-phosphabicyclo[3.3.1]nonane 9-cyclopentyl-9-phosphabicyclo[4.2.1]nonane
https://huagongshe.com/reaction/420831
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | cis,cis-1,5-Cyclooctadiene | HCID 8135 | — |
| Reactant | Butanenitrile, 2,2'-azobis[3-methyl- | HCID 11240960 | — |
| Reactant | Cyclopentylphosphine | HCID 11457667 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 9-Cyclopentyl-9-phosphabicyclo[3.3.1]nonane 9-cyclopentyl-9-phosphabicyclo[4.2.1]nonane | HCID 86634492 | — |
Reaction Steps
A 25 ml stirred vessel was charged at room temperature under nitrogen with 2.0 g (18.5 mmol) of 1,5-cyclooctadiene (Aldrich, 82018 Taufkirchen, DE), 71 mg of azo-bis-isovaleronitrile (VAZO 67, Aldrich, 82018 Taufkirchen, DE) and 3.8 g of a 50% strength solution of monocyclopentylphosphine in toluene (Cytec). This initial charge was subsequently heated to a bath temperature of 80° C. with stirring. After 24 h it was cooled to room temperature, treated with a further 71 mg of AIBN and heated with stirring at a bath temperature of 80° C. for a further 24 h. Subsequently it was worked up by vacuum distillation, giving 2.3 g of cyclopentylphobane isomer mixture (60% of theory; b.p.: 95° C. at 0.05 mbar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08097691B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-8a9efa35c8e34dfc84178de95c777e39 |
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| Source note | uspto-grants-2012_01 |
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