HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 123711379, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1,1,3,3-Tetramethoxy-1,3-dimethyldisiloxane | HCID 87496 | — |
| Reactant | 3-[Methoxy(dimethyl)silyl]propyl 2-methylprop-2-enoate | HCID 3017711 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 123711379 | HCID 123711379 | 82% |
Reaction Steps
A flask was charged with 216 g of γ-methacryloxypropyldimethylmethoxysilane and 500 g of methanol. Under a nitrogen stream, the flask was cooled to 5° C., to which 18.0 g of 0.2N acetic acid was added dropwise over 15 minutes while the liquid temperature was maintained below 10° C. After the completion of dropwise addition, stirring continued for one hour at room temperature. Then, 2260 g of 1,3-dimethyl-1,1,3,3-tetramethoxydisiloxane was added. Stirring continued for 2 hours at room temperature and for a further 8 hours at 60° C. The methanol and volatile matter were removed from the reaction solution by heating in vacuum, obtaining 1-(γ-methacryloxypropyl)-3,5-dimethyl-3,5,5-trimethoxytrisiloxane (M-2) in a yield of 82%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851547B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-e1453f226d19454286f5ba23379e75c4 |
| Source note | uspto-grants-2010_12 |