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HRID 916202作成日:2026年10月26日

Hydrogen Peroxide → [3-[1,3,3,3-Tetramethyl-1-[(trimethylsilyl)oxy]disiloxanyl]propoxy]-propanol

https://huagongshe.com/reaction/916202

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物Magnesium orthosilicateHCID 66225—
反応物Trimethyl-[methyl(trimethylsilyloxy)silyl]oxysilaneHCID 74640—
反応物2-Propanol, 1-(2-propenyloxy)-HCID 542178—
触媒PlatinumHCID 23939—
触媒Chloroplatinic acidHCID 61859—
溶媒MethanolHCID 887—
溶媒IsopropanolHCID 3776—
生成物[3-[1,3,3,3-Tetramethyl-1-[(trimethylsilyl)oxy]disiloxanyl]propoxy]-propanolHCID 22600881—

反応条件

温度80 °C

反応手順

A carbinol functional siloxane having Structure VIII was prepared by hydrosilylation. Specifically, 1.2 parts by weight of 1-allyloxy-2-propanol in the presence of a catalytic amount of chloroplatinic acid (10 ppm platinum as a solution of 7.5% by weight in isopropanol) and 0.004 parts by weight of magnesium silicate was warmed to 80° C. under inert atmosphere. One part by weight 1,1,1,3,5,5,5-heptamethyltrisiloxane was added through an addition funnel over 5 hours. The mixture was treated with 0.02 parts by weight of a 35% solution of aqueous hydrogen peroxide and stirred for two hours at 80° C. Filtration yields [3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]disiloxanyl]propoxy]-propanol (CAS# [77623-99-5]) as a water white liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07268176B2
出典データセットuspto-grants-2007_09
ORD IDord-d70f62c24e994e02984489792aae06a3
出典メモuspto-grants-2007_09