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10
Experimental Procedure:
The reaction of dodec-1-en-11-yne with Ph3SiH is representative.
In a 30 mL round-bottomed flask, Pd2(dba)3·CHCl3 (5.2
mg, 0.005 mmol) and tricyclohexylphosphine (5.6 mg, 0.02 mmol) were
placed under argon atmosphere, and dodec-1-en-11-yne (0.26 mL, 1.2
mmol) was introduced via a syringe. The mixture was stirred well
for 10 min to make it homogeneous. To the mixture, triphenylsilane
(260 mg, 1.0 mmol) was added at room temperature. Triphenylsilane
was soon dissolved and the mixture became homogeneous. After 1 h,
the reaction mixture was submitted on silica gel purification to
provide (E)-1-triphenylsilyl-dodeca-1,11-diene
(369 mg, 0.87 mmol) in 87% yield along with a minor amount
of 2-triphenylsilyl-dodeca-1,11-diene (3%).
11 None of alkenylsilanes were obtained
with triethylsilane.
13
Experimental Procedure
for Aqueous Reaction: In a round-bottomed flask, Pd2(dba)3·CHCl3 (5.2
mg, 0.005 mmol), tris(2,4,6-trimethoxyphenyl)phosphine (10.7 mg, 0.02
mmol), and 1-octyne (0.30 mL, 2.0 mmol) were mixed well. To the
mixture, distilled water (5 mL, non-degassed) was introduced and
the mixture was stirred vigorously (1500 rpm) for 5 min. Triphenylsilane
(260 mg, 1.0 mmol) was then added, and the heterogeneous mixture
was stirred vigorously for 6 h. Extractive workup and purification provided
(E)-1-triphenylsilyl-1-octene (256 mg,
0.69 mmol) along with 2-triphenylsilyl-1-octene (13%).
14 An addition of a small amount of water
(0.1 mL) to the neat reaction did not enhance the reactivity. Therefore,
the amount of water is essential.