tert-Butyldiphenylchlorosilane → Tert-butyl(cyclopent-3-en-1-yloxy)diphenylsilane

Participants

Reaction Steps

By using 2.2 g of 3-cyclopentenol prepared according to the method described in J. Org. Chem., 25, 26-29 (1960) and 9.2 g of t-butyldiphenylsilyl chloride and by the same procedures as in (1) of the intermediate preparation example 1, there was obtained 8.15 g of 3-cyclopenten-1-yl (t-butyldiphenylsilyl) ether. Yield 97%

Provenance & Evidence