Reaction of the diisopropylaminochlorophosphenium cation with crotonaldehyde dimethylhydrazone and acetone azine
β Scribed by Atta M. Arif; Alan H. Cowley; Robert M. Kren; Donald L. Westmoreland
- Book ID
- 102234611
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 384 KB
- Volume
- 1
- Category
- Article
- ISSN
- 1042-7163
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β¦ Synopsis
Abstract
The phosphenium ion [(iβPr~2~N)CIP]^+^ (1) reacts with crotonaldehyde dimethylhydrazone (2) to afford a product with a C~3~NP ring system (4). The reaction of 1 with acetone azine (3) results in a novel tricyclic compound (6) which features a C~2~N~2~P~2~ and two C~2~N~2~P rings. The structures of 4 and 6 were established by Xβray crystallography. Compound 4, C~12~H~26~AlCl~3~N~3~OP, crystallizes in the monoclinic space group __P__2~1~/n with Z = 4, a = 15.400(6), b = 14.442(4), c = 9.206(3) Γ , and Ξ² = 93.33(3)Β°. Compound 6, C~12~H~22~Al~2~Cl~6~N~4~O~2~P~2~, crystallizes in the triclinic group __P__1 with Z = 1, a = 8.556(1), b = 9.782(1), c = 8.119(1) Γ , Ξ± = 94.48(1), Ξ² = 104.97(1), and Ξ³ = 78.35(1)Β°.
π SIMILAR VOLUMES
N-Renzoylperoxycarbamic acid (BPC) was found to react generally with imines and asines to form oxasiridines rather than N-oxides. The imine products were stable, but those found from asines apparently were unstable and converted to ketones or aldehydes plus diazo compounds. N-Bensoylperoxycarbamic a