Isopropanol → HCID 15219056, compound

Reaction equation

[CH:1]1([Si:6]([O:13][CH2:14][CH3:15])([O:10][CH2:11][CH3:12])[O:7][CH2:8][CH3:9])[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:16](O)(C)C.C[Si](C)(C)Cl>[O-]CC.[Na+]>[CH:11]([O:10][Si:6]([CH:1]1[CH2:2][CH2:3][CH2:4][CH2:5]1)([O:13][CH2:14][CH3:15])[O:7][CH2:8][CH3:9])([CH3:16])[CH3:12]

Participants

Procedure

In a 500 ml three-neck flask provided with a magnetic stirrer and a reflux condenser were charged 19.6 g (0.0841 mole) of cyclopentyl triethoxysilane, 98.0 g (1.63 mole) of isopropyl alcohol and 198.7 mg (2.92 m mole) of sodium ethoxide, which were then reacted with each other at room temperature for 2 hours under stirring. Then, trimethylchlorosilane was added to neutralize the alkali. Then, 9.56 g (0.0388 mole) of isopropoxy cyclopentyl diethoxysilane were obtained by vacuum distillation. Its structure was confirmed as in Example 1. Tile yield was 46%.