The hydroboration of benzo-, toluo-, p-methoxybenzo-, or pivalonitriles with bis(9-borabicyclo[3.3.1]nonane)2 (9H-9-BBN)2 affords the corresponding 9-aldimino-9-borabicyclo[3.3.1]nonanes (I) in about 80% yields. Compds. I (R = Ph, CMe3) readily react with and excess of (9H-9-BBN)2 to form the 1:1 adducts II contg. a NB2H four-membered ring (x-ray structure of II, R = Ph was obtained). The adducts II are thermally stable. II, R = Ph, is converted to benzylbis(1,5-cyclooctanediylboryl)amine only after 48 h at reflux in mesitylene. Compds. I are stable towards strong N-bases. I, R = CMe3 reacts with Et2O.BF3 to form 9-fluoro-9-borabicyclo[3.3.1]nonane and the 1:1 cyclic adduct III from (2,2-dimethylpropylideneamino)difluoroborane and I (R = CMe3).
[1]
Koichi Ito,et al.
Synthesis of secondary carbinamine via n-boryl imines generated from nitriles and alkylboranes
,
1992
.
[2]
R. Boese,et al.
9‐Fluor‐9‐borabicyclo[3.3.1]nonan ‐ Charakterisierung in Lösung und im Kristall
,
1990
.
[3]
R. Boese,et al.
Pyrazole‐Organoboranes, VI. Monomeric and Dimeric 9‐Pyrazolyl‐9‐borabicyclo[3.3.1]nonanes
,
1990
.
[4]
R. Köster,et al.
Borverbindungen XLVI. Darstellung von 9‐Borabicyclo[3.3.1]nonanylaminen
,
1977
.
[5]
R. Boese,et al.
Substituted C3BN2 Heterocycles from Trialkylboranes and Nitriles
,
1992
.