Allyl chloride → Trichloropentylsilane

反応式

[CH3:1][CH2:2][C:3]([CH3:5])=C.CC=C(C)C.[Cl:11][SiH:12]([Cl:14])[Cl:13].[CH2:15](Cl)C=C>>[CH2:15]([Si:12]([Cl:14])([Cl:13])[Cl:11])[CH2:5][CH2:3][CH2:2][CH3:1]

参加物

反応物 4

HCID 7850Allyl chloride

HCID 105532-Methyl-2-butene

HCID 112402-Methyl-1-butene

HCID 24811Trichlorosilane2 回

生成物 1

HCID 7885Trichloropentylsilane

実験手順

The process described in Example 2 is repeated, except that 1.5 liters of a mixture prepared from isomeric pentenes (10 percent by weight of 2-methylbutene-1, 82 percent by weight of 2-methylbutene-2 and 8 percent by weight of pentenes having an undetermined structure) and 10 ml of the catalytic solution are substituted for the trichlorosilane, allyl chloride and catalytic solution. About 98.6 percent of the trichlorosilane employed is reacted and 14.5 mol percent per hour of pentyltrichlorosilane is obtained. The product's purity is 92.5 percent by weight as determined by gas chromatography.