[CH2:1]=[C:2]([C:7]#[N:8])[C:3]([C:5]#[N:6])=[CH2:4].C(C#N)CC=[CH:12][CH2:13][CH:14]([C:18]#[N:19])[CH2:15][CH2:16][CH3:17]>C(Cl)Cl>[CH2:3]([C:5]#[N:6])[CH2:2][CH2:1][CH2:1][C:2]([C:7]#[N:8])=[C:3]([C:5]#[N:6])[CH2:4][CH2:12][CH2:13][CH:14]([C:18]#[N:19])[CH2:15][CH2:16][CH3:17]A further preparation employed 1,3-butadiene-2,3-dicarbonitrile in a condensation reaction with 9-oxatricyclo[4.2.12,5.0]non-3-ene-1,6-dicarbonitrile utilizing methylene chloride as diluent under room temperature conditions and a contacting time of about 5 days. By this method, a conversion of about 50 percent was obtained based on the 9-oxatricyclo[4.2.12,5.0]non-3-ene-1,6-dicarbonitrile, resulting in nearly 100 percent ultimate yields of 13-oxatetracyclo[8.2.12,9.0.03,8 ]tridec-5-ene-1,5,6,10-tetracarbonitrile.
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