HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl Methacrylate → Butyl 2-methylprop-2-enoate--methyl 2-methylprop-2-enoate (1/1)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl Methacrylate | HCID 7354 | — |
| Reactant | 2,2,9,9-Tetramethyl-4-(propan-2-ylidene)-3,5,8-trioxa-2,9-disiladecane | HCID 15020093 | — |
| Reactant | HCID 178486114 | HCID 178486114 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Butyl 2-methylprop-2-enoate--methyl 2-methylprop-2-enoate (1/1) | HCID 62798 | — |
Reaction Steps
Following the procedure of Example 46, hydroxy-terminated methyl methacrylate (35%)/n-butyl methacrylate (BMA) (65%) copolymer was prepared using the following amounts of materials: [(2-methyl-1-[2-(trimethylsiloxy)ethoxy]-1-propenyl)oxy]trimethylsilane, 0.51 g (1.85 mmol); MMA, 11 ml (103.7 mmol); BMA, 30 ml (188.5 mmol); tris(dimethylamino)sulfonium bifluoride, 20 mg (0.1 mmol); THF, 100 ml. Upon addition of the monomers the temperature rose to 48.6° from 20.6°. Evaporation of solvents and drying of the resultant residue gave 38.6 g of copolymer. GPC: Mn 22100, Mw 24500, D 1.11 (theor. Mw 20,215).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04417034 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-428f5ffa23e4452e96eee87ad1d6b937 |
| Source note | uspto-grants-1983_11 |