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HRID 30510作成日:2026年10月26日

Cetyl Alcohol → (C16H33O)3Si-C3H6-SH

https://huagongshe.com/reaction/30510

反応式

関与物質

役割名称HCID仕込み量
反応物Cetyl AlcoholHCID 2682—
反応物1-Propanethiol, 3-(triethoxysilyl)-HCID 84658—
触媒TetrabutoxytitaniumHCID 521701—
溶媒EthanolHCID 702—
生成物(C16H33O)3Si-C3H6-SHHCID 22227203—

反応条件

温度105 °C

反応手順

2002.6 g of 3-mercaptopropyl(triethoxy)silane are mixed with 6108.5 g of hexadecanol as well as with 2 g of tetrabutyl orthotitanate and heated at 95-115° C. for 360 minutes in a 10 liter flask in a distillation apparatus. Ethanol formed in the transesterification is distilled off in vacuo at 15-600 mbar. After cooling, 7022 g of a colourless, solid product are obtained. As can be shown by 1H-NMR and 29Si-NMR, 92% of the EtO—Si groups are replaced by R—O—Si. In the transesterification more than 80 mole % of the ethanol-free compound [(C16H33O)3Si—C3H6—SH is formed, as can be shown for example by 1H-NMR and 29Si-NMR.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07423165B2
出典データセットuspto-grants-2008_09
ORD IDord-3994d8fbc2414735b1726cfcc0b8241d
出典メモuspto-grants-2008_09