돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704842생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물Allyl methacrylateHCID 7274—
반응물SilaneHCID 23953—
반응물Trimethyl-[methyl(trimethylsilyloxy)silyl]oxysilaneHCID 74640—
촉매Chloroplatinic acidHCID 61859—
용매IsopropanolHCID 3776—
생성물2-Propenoic acid, 2-methyl-, 3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]-1-disiloxanyl]propyl esterHCID 88005—

반응 조건

온도70 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04988788
출처 데이터셋uspto-grants-1991_01
ORD IDord-3da27bda073541c391b39d95b23b01c1
출처 메모uspto-grants-1991_01