Hydrochloric Acid → Triisopropylsilyl chloride
Reaction equation
[CH:1]([Si:4]([CH:10]([CH3:12])[CH3:11])([CH:7]([CH3:9])[CH3:8])OC)([CH3:3])[CH3:2].[ClH:13]>>[CH:1]([Si:4]([CH:10]([CH3:12])[CH3:11])([CH:7]([CH3:9])[CH3:8])[Cl:13])([CH3:3])[CH3:2]Participants
3
Conditions
- Temperature
- 20 °C
Procedure
A 500 ml-capacity, four-necked flask fitted with a stirrer, a thermometer and a Dimroth was charged with 37.7 g (0.2 moles) of triisopropylmethoxysilane. To the flask was then added 150 g of 35% hydrochloric acid, and the resulting mixture was stirred at 20° C. for 10 hours to effect the reaction. The resulting reaction solution was separated into the aqueous layer and the organic layer. The organic layer was distilled to afford 38 g of triisopropylchlorosilane as a fraction boiling at 78° C.-80° C./10 mm Hg (yield; 99%).
Workup
- customA 500 ml-capacity, four-necked flask fitted with a stirrer
- customthe reaction
- customThe resulting reaction solution
- customwas separated into the aqueous layer
- distillationThe organic layer was distilled
Sources & evidence
- ORD record
- ord-f20e4d408cff4fbfbd0c8118dca03797
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07459577B2
Reaction notes
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