1-Butanol → Butoxy(triethyl)silane
Reaction equation
[CH2:1]([OH:5])[CH2:2][CH2:3][CH3:4].[CH2:6]([Si:8]([CH2:12][CH3:13])([CH2:10][CH3:11])Cl)[CH3:7].Cl>[Cl-].C([N+](CC)(CC)CC1C=CC=CC=1)C.CC1C=CC(C)=CC=1>[CH2:1]([O:5][Si:8]([CH2:12][CH3:13])([CH2:10][CH3:11])[CH2:6][CH3:7])[CH2:2][CH2:3][CH3:4]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
0.1 moles of n-butanol, 0.15 moles of triethylchlorosilane and 0.0005 moles of triethylbenzyl ammonium chloride in 50 ml of p-xylene were heated under reflux (80°-110° C.). When the evolution of HCl had ceased, the product was worked up by fractional distillation at reduced pressure.
Workup
- temperatureunder reflux (80°-110° C.)
- distillationthe product was worked up by fractional distillation at reduced pressure
Sources & evidence
- ORD record
- ord-adda96e4f7b048839a4c5ba7b0701f31
- Source dataset
- uspto-grants-1992_08
- Patent number
- US05142081
Reaction notes
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