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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Allyl methacrylate | HCID 7274 | — |
| Reactant | Silane | HCID 23953 | — |
| Reactant | Trimethyl-[methyl(trimethylsilyloxy)silyl]oxysilane | HCID 74640 | — |
| Catalyst | Chloroplatinic acid | HCID 61859 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 2-Propenoic acid, 2-methyl-, 3-[1,3,3,3-tetramethyl-1-[(trimethylsilyl)oxy]-1-disiloxanyl]propyl ester | HCID 88005 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988788 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-3da27bda073541c391b39d95b23b01c1 |
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| Source note | uspto-grants-1991_01 |
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