[CH:1]1[CH2:8][CH2:7][CH:6]=[CH:5][CH2:4][CH2:3][CH:2]=1.N(C(C(C)C)C#N)=NC(C(C)C)C#N.[CH:23]1([PH2:28])[CH2:27][CH2:26][CH2:25][CH2:24]1.CC(N=NC(C#N)(C)C)(C#N)C>C1(C)C=CC=CC=1>[CH:23]1([P:28]2[CH:5]3[CH2:6][CH2:7][CH2:8][CH:1]2[CH2:2][CH2:3][CH2:4]3)[CH2:27][CH2:26][CH2:25][CH2:24]1.[CH:23]1([P:28]2[CH:6]3[CH2:7][CH2:8][CH:1]2[CH2:2][CH2:3][CH2:4][CH2:5]3)[CH2:27][CH2:26][CH2:25][CH2:24]1A 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).
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