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Allyl chloride → Trichloropentylsilane
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Allyl chloride | HCID 7850 | — |
| 反応物 | 2-Methyl-2-butene | HCID 10553 | — |
| 反応物 | 2-Methyl-1-butene | HCID 11240 | — |
| 反応物 | Trichlorosilane | HCID 24811 | — |
| 生成物 | Trichloropentylsilane | HCID 7885 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04276426 |
| 出典データセット | uspto-grants-1981_06 |
| ORD ID | ord-1177e3ebc13a4116a33f2b4ee92fe20a |
| 出典メモ | uspto-grants-1981_06 |