sufficieiit to prepare a n isolable quantity of the ketone. A few milligrams of the imine was hydrolyzed :rnd the product yielded a 2,4-dinitrophenylhydrazone, m.p. 138", calctl for C L ~ S ? 6 S 4 ON, 4 : 13.65; found: S , 13.50.
TABLE I11
c E-12'\
KETONES
I
H3C-- C--C 0-- I< /
,'
(CH,, )!CH----HC--- -C1Is C'arbon,
IZ n-Butyl Icobntyl s-Butyl Isoamyl Phenyla
" The
B.B.
" C . (mm.! 97-99 (1) 83-87 I I J
104
(ij)
1% -122 (6:
c;
I P ~ ii%i Calcd. Found 0.8793 1.4843 7 9 . 9 3 79.95 ,8763 1 . G 2 7 7!l.U:3 iS.53 .H791 I 4.53'1 7Ir.93 7!l 5 9 87ii9 1 80 29 $O.?(i
IJydrogen, I ' (