Synthesis of phosphine-borane complexes of P-heterocycles

• Published in: Journal of organometallic chemistry Vol. 516; no. 1; pp. 139 - 145
• Main Authors: Keglevich, György, Újszászy, Kálmán, Szöllősy, Áron, Ludányi, Krisztina, Tőke, László
• Format: Journal Article
• Language: English
• Published: LAUSANNE 1 Elsevier B.V 14.06.1996; Elsevier
• Subjects: Chemistry; Chemistry, Inorganic & Nuclear; Chemistry, Organic; Dichlorocarbene; Dihydro-1H-phosphole; Dihydrophosphinine; Phosphabicyclohexane; Phosphepine; Phosphine-borane complex; Physical Sciences; Science & Technology; Dihydro-1H-phosphole; Phosphabicyclohexane; Phosphine-borane complex; Dichlorocarbene; Dihydrophosphinine; Phosphepine; phosphabicyclohexane; dichlorocarbene; 1-OXIDES; phosphine-borane complex; dihydrophosphinine; phosphepine; dihydro-1H-phosphole
• ISSN: 0022-328X; 1872-8561
• DOI: 10.1016/0022-328X(96)06134-7

Dihydro-1H-phosphole-boranes 5 and 10 were prepared from phosphine oxides 1 and 9 respectively. Reaction of borane 5 with dichlorocarbene gave dihydrophosphole-dichloromethylborane 6 and tetrahydro derivative 7a as the main products, and dichlorocyclopropane 8 as the minor component. Dichlorocarbene addition reaction of boranes 10 did not afford the corresponding phosphabicyclohexanes, but the dichloromethylborane complexes of the dihydro- and tetrahydrophospholes ( 11 and 7 respectively). Phosphabicyclohexaneborane 13 was synthesized from P-oxide 12 by change in the functionality. The dihydrophosphinine-boranes ( 16) were prepared by cyclopropane ring opening of phosphabicyclohexane 13, or by change in the functionality of P-oxide 15. Reaction of dihydrophosphinine-boranes 17 with dichlorocarbene gave traces of dihydrophosphinine-dichloromethylborane 18 instead of the phosphepine. The phosphepine-borane ( 20) was synthesised from oxide 19. The preparation of unsaturated phosphine-boranes was complicated by reduction side-reactions. The products were characterized by 31P, 11B, 1H and 13C NMR, as well as MS data.