HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399884Generated: October 26, 2026
2-Methylbenzenesulfonic acid → HCID 18326000, compound
https://huagongshe.com/reaction/399884
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylbenzenesulfonic acid | HCID 6925 | — |
| Reactant | Methacrylic anhydride | HCID 12974 | — |
| Reactant | 4-Ethylphenyl 4-hydroxybenzoate | HCID 13719873 | — |
| Reactant | 4-Ethylphenyl 4-trimethylsilyloxybenzoate | HCID 53950183 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 18326000 | HCID 18326000 | — |
Reaction Steps
A solution of 16.9 g of 4-ethylphenyl 4-trimethylsilyloxybenzoate (prepared according to the instructions in EP-A-0 358 205, page 9, section C) in 15 ml of toluene and 10 ml of ethanol was boiled under reflux for one hour and then freed from volatile constituents by heating at 100° C. for 60 minutes. The 13.3 g of 4-ethylphenyl 4-hydroxybenzoate which remained were dissolved, together with 30 g of methacrylic anhydride and 1.2 g of toluenesulfonic acid, in 15 ml of toluene and the solution was heated at 100° C. for 1 hour. After cooling, the product was precipitated with hexane and recrystallized from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05824733 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-6b267d8fecba4701972798274e4568d9 |
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| Source note | uspto-grants-1998_10 |
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