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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704842Generated: October 25, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl methacrylateHCID 7274—
ReactantSilaneHCID 23953—
ReactantTrimethyl-[methyl(trimethylsilyloxy)silyl]oxysilaneHCID 74640—
CatalystChloroplatinic acidHCID 61859—
SolventIsopropanolHCID 3776—
Product2-Propenoic acid, 2-methyl-, 3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]-1-disiloxanyl]propyl esterHCID 88005—

Reaction Conditions

Temperature70 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988788
Source datasetuspto-grants-1991_01
ORD IDord-3da27bda073541c391b39d95b23b01c1
Source noteuspto-grants-1991_01