Issue 8, 1981

Synthesis, stereochemistry, and crystal and molecular structure of 4-bromo-1,2,2,3-tetramethyl-1-phenylphosphetanium bromide

Abstract

The synthesis of 4-bromo-2,2,3-trimethyl-1-phenylphosphetan 1-oxide was achieved by reaction of 1-bromo-3,3-dimethylbut-1-ene with phenylphonous dichloride in the presence of anhydrous aluminium chloride, followed by the addition of water. The oxide was converted into the title compound by reduction (Cl3SiH) and then quaternization with methyl bromide. The title compound crystallizes in the monoclinic space group P21/n, with four molecules in a unit cell of dimensions a= 7.653(1), b= 12.662(3), c= 15.487(3)Å and β= 97.58(2°). The structure was solved by the heavy-atom method and refined to a final R value of 0.065. The four-membered ring is puckered with a dihedral angle of 34.0°. The methyl substituent at C(3) and the phenyl group have a cis-relation, whereas the bromo-substituent and phenyl ring are trans. All three of these groups occupy equatorial positions with respect to the ring.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1981, 1138-1142

Synthesis, stereochemistry, and crystal and molecular structure of 4-bromo-1,2,2,3-tetramethyl-1-phenylphosphetanium bromide

Mazhar-ul-Haque, W. Horne, S. E. Cremer, P. W. Kremer and P. K. Kafarski, J. Chem. Soc., Perkin Trans. 2, 1981, 1138 DOI: 10.1039/P29810001138

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