Role of neighboring groups in replacement reactions. XXIX. 5

Endothelin-Converting Enzyme-1 Inhibition and Growth of Human Glioblastoma Cells ... A Butyrolactone → 1,3-diol Strategy for the Obtention ofTolypot...
0 downloads 0 Views 504KB Size
4008

Based on this kinetic scheme, the following relationships for I P are apparent.

krp = klp(F) kt, = k l d 1 - F) kr, t kt,

+

=

+ kt, kl, kms + kts = kis

km,

=

k-2

(29)

(30)

kz( R+X-)

(R+\lX-) =

(28)

(R+X-)

krs kts = (3 1) Similarly, eq 31 can be written for the IS ester. Steady-State Concentrations for Solvolysis Scheme 1. Application of the usual steady-state approximation to solvolysis Scheme I gives relations 32, 33, and 34 for the steady-state concentrations of R+, R+I/X-, and R+X-, respectively.

+ kslI1

(33) ksIV k3k-3(X-) ksIv

+

=

ki(RX) k-z k-2

I

ksIV + kslI1+ k3k-3(X-) + ksIV

(34)

The Role of Neighboring Groups in Replacement Reactions. XXIX. 5-Methoxyl Participation and Lithium Aluminum Hydride Reduction' Evan L. Allred and S. Winstein

Contribution No. 2055 f r o m the Department of Chemistry, University of California, Los Angeles, California 90024, and the Department of Chemistry, Unicersity of Utah, Salt Lake City, Utah. Received February 25, 1967 Abstract: Reduction of 4-methoxy-1-pentyl (IP) and 5-methoxy-2-pentyl (IS) p-bromobenzenesulfonates with lithium aluminum hdyride in ether solvent results in formation of rearranged methyl pentyl ether, 2-methyltetrahydrofuran, and unrearranged methyl pentyl ether. The mechanistic implications are discussed; the results are considered to be consistent with salt-promoted anchimerically assisted ionization and fit in the N category of the N-Lim mechanism spectrum. ince complex metal hydrides were first introduced as reducing agents, 2 , 3 several aralkyl and alkyl arenesulfonate and halide systems have been observed to yield appreciable amounts of rearranged hydrocarbons as a consequence of r e d u ~ t i o n . " ~ These reductions are clearly the result of neighboring group participation, and in most cases appear to follow anchimerically assisted ionization. However, to date, little attention has been given to the mechanistic details for such product formation. In this regard, the reductions of 4methoxy-1-pentyl (IP) and 5-methoxy-2-pentyl (IS) p-bromobenzenesulfonates are informative. It has been observed that both I P and IS give rearranged methyl pentyl ether and 2-methyltetrahydrofuran as well as unrearranged methyl pentyl ether when reduced with lithium aluminum hydride in ether.1° Thus with the same molecular species reduction involves reaction

S

(1) This research supported by the National Science Foundation. (2) A. E. Finholt, A. C. Bond, and H. I. Schlesinger, J . A m . Chem. Soc., 69, 1199 (1947). (3) R. F. Nystrom and W. G. Brown, ibid., 69, 1197 (1947). (4) D. J. Cram, ibid., 74, 2149, 2152 (1952). (5) H. Schmid and P. Karrer, Helc. Chim. Acta, 32, 1371 (1949). (6) E. J. Corey, M. G. Howell, A. Boston, R. L. Young, and R. A. Sneen, J . A m . Chem. Soc., 78, 5036 (1956). (7) P. R. Story, ibid., 83, 3348 (1961); P. R. Story and M. Saunders, ibid., 84, 4876 (1962). (8) H. C. Brown and H. M. Bell, ibid., 85, 2324 (1963). (9) S. Winstein, A. H. Lewin, and I