Reaction #6544

ord-44523718c32f4f8db78be90afe1a804e

Reaction equation

CO[Si](OC)(OC)C1CCCC1
cyclopentyl trimethoxysilane
CCC(C)(C)O
tert-amyl alcohol
C[Si](C)(C)Cl
trimethylchlorosilane
CCC(C)(C)O[Si](OC)(OC)C1CCCC1
tert-amyloxy cyclopentyl dimethoxysilane
Yield 82.0%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    OtherIn a 100 ml three-neck flask provided with a magnetic stirrer and a reflux condenser
  2. 2
    Otherwere then reacted with each other in an oil bath of 105° C. for 4 hours

Procedure

In a 100 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 10.1 g (0.0531 mole) of cyclopentyl trimethoxysilane, 30.6 g (0.347 mole) of tert-amyl alcohol and 86.4 mg (1.6 m mole) of sodium methoxide, which were then reacted with each other in an oil bath of 105° C. for 4 hours under stirring. Then, trimethylchlorosilane was added to neutralize the alkali. Then, 10.7 g (0.0434 mole) of tert-amyloxy cyclopentyl dimethoxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. The yield was 82%.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05248803uspto-grants-1993_09