Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
Reactantcis,cis-1,5-CyclooctadieneHCID 8135—
ReactantButanenitrile, 2,2'-azobis[3-methyl-HCID 11240960—
ReactantCyclopentylphosphineHCID 11457667—
SolventTolueneHCID 1140—
Product9-Cyclopentyl-9-phosphabicyclo[3.3.1]nonane 9-cyclopentyl-9-phosphabicyclo[4.2.1]nonaneHCID 86634492—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08097691B2
Source datasetuspto-grants-2012_01
ORD IDord-8a9efa35c8e34dfc84178de95c777e39
Source noteuspto-grants-2012_01