HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379378Generated: October 25, 2026
2-Methylbenzenesulfonic acid → HCID 18326000, compound
https://huagongshe.com/reaction/2379378
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 by the procedure in EP-A-358,208, page 9, sec. C) in 15 ml of toluene and 10 ml of ethanol was refluxed for 1 hour and then freed from volatile components by heating at 100° C. for 60 minutes. The remaining 13.3 g of 4-ethylphenyl 4-hydroxybenzoate were dissolved in 15 ml of toluene together with 30 g of methacrylic anhydride and 1.2 g of toluenesulfonic acid, and the mixture 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 | US05362315 |
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| Source dataset | uspto-grants-1994_11 |
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| ORD ID | ord-702f6a7665d840f99fd64dc626ae4b28 |
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| Source note | uspto-grants-1994_11 |
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