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Easy Access to Phosphine-Borane Building Blocks.


ABSTRACT: In this paper, we highlight the synthesis of a variety of primary phosphine-boranes (RPH2 ?BH3 ) from the corresponding dichlorophosphines, simply by using Li[BH4 ] as reductant and provider of the BH3 protecting group. The method offers facile access not only to alkyl- and arylphosphine-boranes, but also to aminophosphine-boranes (R2 NPH2 ?BH3 ) that are convenient building blocks but without the protecting BH3 moiety thermally labile and notoriously difficult to handle. The borane-protected primary phosphines can be doubly deprotonated using n-butyllithium to provide soluble phosphanediides Li2 [RP?BH3 ] of which the phenyl-derivative Li2 [PhP?BH3 ] was structurally characterized in the solid state.

SUBMITTER: de Jong GB 

PROVIDER: S-EPMC7756754 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature

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Easy Access to Phosphine-Borane Building Blocks.

de Jong G Bas GB   Ortega Nuria N   Lutz Martin M   Lammertsma Koop K   Slootweg J Chris JC  

Chemistry (Weinheim an der Bergstrasse, Germany) 20201023 68


In this paper, we highlight the synthesis of a variety of primary phosphine-boranes (RPH<sub>2</sub> ⋅BH<sub>3</sub> ) from the corresponding dichlorophosphines, simply by using Li[BH<sub>4</sub> ] as reductant and provider of the BH<sub>3</sub> protecting group. The method offers facile access not only to alkyl- and arylphosphine-boranes, but also to aminophosphine-boranes (R<sub>2</sub> NPH<sub>2</sub> ⋅BH<sub>3</sub> ) that are convenient building blocks but without the protecting BH<sub>3</s  ...[more]

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