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HRID 617106作成日:2026年10月26日

Hexane → Methyl octadecyl-chlorosilane

https://huagongshe.com/reaction/617106

反応式

関与物質

役割名称HCID仕込み量
反応物HexaneHCID 8058—
反応物But-3-enyl(dichloro)silaneHCID 57372819—
反応物HCID 178442891HCID 178442891—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl octadecyl-chlorosilaneHCID 57347242—

反応手順

[(CH3)2N--Si--(CH3)--C18H37)CH2 ]2CH2 was prepared as follows. Allylmethyldichlorosilane (0.69 moles, available from the Aldrich Chemical Co., Milwaukee, Wis., USA) was put into a reaction flask with 250 milliliters of tetrahydrofuran (THF). One molar octadecylmagnesium chloride (0.65 moles) in THF was added portionwise to the flask while the mixture was stirred and cooling to a temperature range of about -10° to +5°. The temperature of this mixture was allowed to increase to 24°. Hexane was added to the mixture, and the solid filtered off. The filtrate was evaporated on a rotary evaporator to leave an oil. The oil was vacuum-distilled, providing 134.7 g (55.8% relative to the theoretical yield) of ally methyl octadecyl-chlorosilane (compound A) as a clear, colorless oil. The boiling point of compound A was 188°/0.1-191°/0.2 mm, and gas chromatography/mass spectrometry (GC/MS) showed 100% compound A.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05948531
出典データセットuspto-grants-1999_09
ORD IDord-4045afe49fe04f68b26f2f1f2cf21528
出典メモuspto-grants-1999_09