HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604609Generated: November 1, 2026
Methyl Methacrylate → HCID 178506799, compound
https://huagongshe.com/reaction/1604609
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl Methacrylate | HCID 6658 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | Isobornylmethacrylate | HCID 71311141 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Lithium Chloride | HCID 433294 | — |
| Product | HCID 178506799 | HCID 178506799 | — |
Reaction Steps
1 ml t-BuLi was added to 40 ml THF containing 3 ml DPE solution (0.392N) in cyclohexane and 2 ml LiCl solution at 0° C. The solution was then brought to the reaction temperature (from -78 to 40° C.), 3 ml of IBMA was added and allowed to polymerize for about 1 hour. Polymer was recovered by precipitation in 200 ml methanol. Note: here the reaction product of t-BuLi and DPE, that is 1,1-diphenyl-3,3-dimethylbutyl lithium (DDBLi), was used as an iniiator. As an alternative example, trimethylsilyl-methyllithium ((Me)3SiCH2Li) was used to directly polymerize IBMA without reacting with DPE. PIBMA of Mn as high as 100,000 with very narrow molecular weight range (<1.15) was obtained at temperature from -78 to 25° C. This is very interesting, since PMMA of narrow Mn distribution can only be obtained at temperature lower than -60° C. by usual anionic polymerization techniques, even with sterically hindered initiator, such as DDBLi, whereas trimethylsilymethyllithium is not very sterically hindered and still produces PIBMA of very narrow Mn distribution at room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994446 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-8432930a02d84c29aa51a7d2c02ff4dd |
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| Source note | uspto-grants-1999_11 |
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