HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341722Generated: October 26, 2026
Methanol → Trimethylsilylmethyl methacrylate dimethylbenzyl methacrylate
https://huagongshe.com/reaction/341722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | Methacryloxymethyltrimethylsilane | HCID 2760855 | — |
| Reactant | 2-Phenylpropan-2-yl 2-methylprop-2-enoate | HCID 15793116 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Trimethylsilylmethyl methacrylate dimethylbenzyl methacrylate | HCID 86753510 | 60% |
Reaction Steps
Trimethylsilylmethyl methacrylate (TMSMMA) and dimethylbenzyl methacrylate (DBMA) were mixed in a ratio of 1:1 so as to prepare a toluene solution having a monomer concentration of 5.0 mol/liter. Next, 2 mol %, on the basis of the monomer of the toluene solution, of 2,2'-azobis(isobutylonitrile) (AIBN) was added to the solution, and the mixture was retained in an oil bath at 80° C. for 8 hours with stirring. Next, the mixture was left standing to cool at room temperature, was diluted with toluene and was thereafter dropped into large quantities of a methanol solution. The resulting precipitate was filtered and dried to obtain a base polymer as a resist material. There was thus obtained a trimethylsilylmethyl methacrylate/dimethylbenzyl methacrylate copolymer represented by the following formula, ##STR11## wherein each of m and n is a positive integer. In this example, the copolymer described above could be obtained at a yield of 60%, the molecular weight was 27,000 and the dispersion was 1.61.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05856071 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-f0a2053055f94cdca01b38a00b7e9686 |
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| Source note | uspto-grants-1999_01 |
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