Hydrogen Bromide → HCID 19875555, compound
Reaction equation
[CH3:1][SiH:2]([CH:6]([CH3:8])[CH3:7])[CH:3]([CH3:5])[CH3:4].[Br:9]Br.Br>>[CH3:1][Si:2]([CH:6]([CH3:8])[CH3:7])([CH:3]([CH3:5])[CH3:4])[Br:9]Participants
4
Procedure
20.8 g (0.16 mol) of the methyldiisopropylsilane prepared under Example 2, above, was placed in a 50 mL three-neck flask equipped with a reflux condenser, thermometer, and addition funnel. 25 g bromine (0.16 mol) was cautiously dripped in while cooling with ice and stirring with a magnetic stirring bar. A strong exothermic reaction developed, and hydrogen bromide was evolved. After addition of the entire quantity of bromine, the reaction was allowed to stand for 1 hour at room temperature and was then distilled in vacuo. 26.3 g (0.13 mol) of the target methyldiisopropylbromosilane (bp=92 degrees Centigrade/50 mmHg) was obtained.
Workup
- customabove, was placed in a 50 mL three-neck flask
- customequipped with a reflux condenser
- additionthermometer, and addition funnel
- temperaturewhile cooling with ice
- customA strong exothermic reaction
- distillationwas then distilled in vacuo
Sources & evidence
- ORD record
- ord-e0f68176a9314f7ea36a566c87dc22da
- Source dataset
- uspto-grants-1992_08
- Patent number
- US05136074
Reaction notes
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