Acetylene → 1,1,3,3-Tetrachloro-1,3-disilacyclopent-4-ene
Reaction equation
[CH:1]#[CH:2].[Cl:3][SiH:4]([CH2:6][SiH:7]([Cl:9])[Cl:8])[Cl:5]>C1C=CC=CC=1>[Cl:3][Si:4]1([Cl:5])[CH:2]=[CH:1][Si:7]([Cl:9])([Cl:8])[CH2:6]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Hydrosilation of acetylene with bis(dichlorosilyl)methane in the presence of RhCl(PPh3)3. Into the same apparatus as described in Example 1 were placed 1.02 g of bis(dichlorosilyl)methane, 0.102 g of RhCl(PPh3)3, and 20 ml of dried benzene. Acetylene gas was blown into the flask at 90 ml/min for 2 hours. The products were vacuum distilled at 67 Pa to yield a mixture comprising 0.61 g of 1,1,3,3-tetrachloro-1,3-disilacyclopent-4-ene (TCD-GC area 3.7%) and 1,1,3,3-tetrachloro-1,3-disilacyclopentane (TCD-GC area 35.6%).
Workup
- distillationdistilled at 67 Pa
Sources & evidence
- ORD record
- ord-efc73f1f701548eb9ac7b4f8898dee0a
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998649
Reaction notes
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