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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372697Generated: October 30, 2026

Benzoyl Peroxide → HCID 86745591, compound

https://huagongshe.com/reaction/2372697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantEthyl MethacrylateHCID 7343—
ReactantHexaneHCID 8058—
ReactantTributyltin methacrylateHCID 16682828—
SolventO-XyleneHCID 7237—
ProductHCID 86745591HCID 86745591—

Reaction Steps

Methacrylic acid (0.1 mol) and tri-n-butylhydroxystannane (0.1 mol) were dissolved in xylene and subjected to reaction. The water that formed as the reaction proceeded was removed together with the solvent by distillation. The by-product of the reaction was distilled off under vacuum and the residue was dried under vacuum to obtain tri-n-butylstannyl methacrylate (m.p. 46° C.; yield, 64%). This tri-n-butylstannyl methacrylate and ethyl methacrylate were put into a round-bottom flask at a molar ratio of 1:1 and xylene was added to achieve a concentration of ca. 50%. Benzoyl peroxide (1 mol % of the sum of tri-n-butylstannyl methacrylate and ethyl methacrylate) dissolved in xylene was charged into a dropping funnel. After equipping the flask with this funnel, the benzoyl peroxide solution was dripped in an amount of about 10% of the total quantity of the solution. Thereafter, the flask was heated to the reflux temperature and the remaining polymerization initiator was slowly added dropwise until the reaction was completed in 8 hours. After the reaction, the content of the flask was added to n-hexane and subjected to re-precipitation. The resulting precipitate was recovered and dried to obtain a solid product, which was slowly added to ice water and reprecipitated. The precipitate was recovered and dried to obtain poly(tri-n-butylstannyl methacrylate-ethyl methacrylate). Yield, 80%, Mn, 48,000; Mw/Mn=1.9, IR (ν cm-1), 1720, 1160, 760, 700; atomic absorption spectrum (Sn content), 24.90 (found) and 24.98 (calculated).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05100762
Source datasetuspto-grants-1992_03
ORD IDord-33390f6736414f3e9d8f340cd07ddf23
Source noteuspto-grants-1992_03