Trichlorosilane → Silane, chlorodimethyl[(trichlorosilyl)methyl]-
Reaction equation
Cl[CH2:2][Si:3]([CH3:6])([CH3:5])[Cl:4].[Cl:7][SiH:8]([Cl:10])[Cl:9]>[Cl-].C([P+](CCCC)(CCCC)CCCC)CCC>[Cl:7][Si:8]([Cl:10])([Cl:9])[CH2:2][Si:3]([Cl:4])([CH3:6])[CH3:5]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In the same apparatus and procedure as Example 1 above, 0.27 g (1.5 mmol) of tetrabutylphosphonium chloride, 2.15 g (15.0 mmol) of (chloromethyl)dimethylchlorosilane, and 6.10 g (45.0 mmol) of trichlorosilane were reacted at 150° C. for 10 hrs. The resulting mixture was distilled to give 2.18 g of 1,1,1,3-tetrachloro-3-methyl-1,3-disilabutane (yield; 60%).
Workup
- distillationThe resulting mixture was distilled
Sources & evidence
- ORD record
- ord-d9d7105fbe1144b2b5829cd024e323a6
- Source dataset
- uspto-grants-2002_05
- Patent number
- US06392077B1
Reaction notes
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