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HRID 704842作成日:2026年10月27日

Allyl methacrylate → 2-Propenoic acid, 2-methyl-, 3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]-1-disiloxanyl]propyl ester

https://huagongshe.com/reaction/704842

反応式

関与物質

役割名称HCID仕込み量
反応物Allyl methacrylateHCID 7274—
反応物SilaneHCID 23953—
反応物Trimethyl-[methyl(trimethylsilyloxy)silyl]oxysilaneHCID 74640—
触媒Chloroplatinic acidHCID 61859—
溶媒IsopropanolHCID 3776—
生成物2-Propenoic acid, 2-methyl-, 3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]-1-disiloxanyl]propyl esterHCID 88005—

反応条件

温度70 °C

反応手順

Into 63 parts of allyl methacrylate admixed with 0.04 part of chloroplatinic acid in the form of an isopropyl alcohol solution and heated at 60° 70° C. were added dropwise gradually 111 parts of 1,1,1,3,5,5,5-heptamethyl trisiloxane and, after completion of the dropwise addition of the silane compound, the mixture was heated at 90° C. for further 2 hours to complete the reaction. Thereafter, the reaction mixture was distilled under reduced pressure to be freed from the unreacted reactants and then filtered to give 1,1,1,3,5,5,5- heptamethyl-3-(3-methacryloxypropyl) trisiloxane, which is referred to as the compound B-1 hereinbelow, in a yield of 165 parts corresponding to 95% of the theoretical yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04988788
出典データセットuspto-grants-1991_01
ORD IDord-3da27bda073541c391b39d95b23b01c1
出典メモuspto-grants-1991_01