TY - JOUR
T1 - Synthesis, stereochemistry, and crystal and molecular structure of 4-bromo-1,2,2,3-tetramethyl-1-phenylphosphetanium bromide
AU - Mazhar-ul-Haque,
AU - Horne, William
AU - Cremer, Sheldon E.
AU - Kremer, Paul W.
AU - Kafarski, Pawel K.
PY - 1981
Y1 - 1981
N2 - 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) A° 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.
AB - 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) A° 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.
UR - https://www.scopus.com/pages/publications/2842611537
U2 - 10.1039/p29810001138
DO - 10.1039/p29810001138
M3 - Article
AN - SCOPUS:2842611537
SN - 0300-9580
SP - 1138
EP - 1142
JO - Journal of the Chemical Society. Perkin Transactions 2
JF - Journal of the Chemical Society. Perkin Transactions 2
IS - 8
ER -