HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 616709Generated: October 29, 2026
Methacrylic Acid → HCID 20273141, compound
https://huagongshe.com/reaction/616709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methacrylic Acid | HCID 4093 | — |
| Reactant | Methyl Methacrylate | HCID 6658 | — |
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Tributyltin hydroxide | HCID 6336496 | — |
| Reactant | 2155-70-6 | HCID 21946344 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 20273141 | HCID 20273141 | — |
Reaction Steps
The monomers of P30 were first synthesized. Tri-n-butyltin methacrylate prepared according to Montermoso et al U.S. Pat. No. 3,016,369. Uninhibited methacrylic acid (37.8 ml, 0.444 mole) and tri-n-butyltin oxide (112.5 ml, 0.222 mole) were reacted in 200 of dischloromethane. Upon refluxing for 1 hour, 4.5 ml of water were collected azeotropically. After the reaction was completed, the solvent was evaporated under vacuum. The product ester was a yellow transparent liquid. The monomers were then copolymerized in a 1-liter, 3-necked flask equipped with a reflux condenser, a thermometer, such that it read the temperature of the reactants, and a mechanical stirrer. Tri-n-butyltin methacrylate (50 grams, 0.140 mole), uninhibited methyl methacrylate (50 grams, 0.580 mole), and benzoyl peroxide (0.5% by weight) were reacted in 200 ml of benzene. The solution polymerization was allowed to reflux for 8 hours. The resultant polymer was clear and could be cast as a film from the benzene solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04075319 |
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| Source dataset | uspto-grants-1978_02 |
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| ORD ID | ord-700fc3a3c4424fba9af17898bbf63163 |
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| Source note | uspto-grants-1978_02 |
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