Methyldichlorosilane → Dichloro(methyl)(2-phenylpropyl)silane
Reaction equation
[CH3:1][SiH:2]([Cl:4])[Cl:3].Cl[SiH](Cl)Cl.[CH2:9](Cl)C=C.C[C:14]1([CH:21]=[CH:20][CH:19]=[CH:18][CH2:17]1)[CH:15]=[CH2:16]>>[C:14]1([CH:15]([CH3:16])[CH2:1][Si:2]([CH3:9])([Cl:4])[Cl:3])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1Participants
5
Procedure
The process described in Example 2 is repeated, except that 1.3 liters of methyldichlorosilane, 1.7 liters of 1-methylstyrene and 5 ml of the catalytic solution are substituted for the trichlorosilane, allyl chloride and catalytic solution and the process is carried out at a temperature of 140° C. instead of 120° C. About 97.9 mol percent of the methyldichlorosilane used is converted and 12.8 moles per hour of 2-phenyl-2-methylethyl (methyl) dichlorosilane are obtained having a purity of 97.2 percent by weight as determined by gas chromatography.
Workup
- customis carried out at a temperature of 140° C. instead of 120° C
Sources & evidence
- ORD record
- ord-a9893f0bfb7241fdab297ba0c4e34031
- Source dataset
- uspto-grants-1981_06
- Patent number
- US04276426
Reaction notes
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