HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156420Generated: October 26, 2026
Triethylamine → 4-((Methylamino)sulfonyl)phenyl 2-methyl-2-propenoate
https://huagongshe.com/reaction/1156420
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methacryloyl chloride | HCID 13528 | — |
| Reactant | 4-hydroxy-N-methylbenzenesulfonamide | HCID 76502 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-((Methylamino)sulfonyl)phenyl 2-methyl-2-propenoate | HCID 18668415 | 79.9% |
Reaction Steps
To a solution of 15.00 g (0.08 mole) of N-methyl-4-hydroxybenzenesulfonamide, 8.11 g (0.08 mole) of triethylamine and 200 ml of methylene chloride cooled to 0° C. was added a solution of 8.37 g (0.08 mole) of methacryloyl chloride in 100 ml of methylene chloride over a period of approximately 30 minutes. The solution was then stirred for another 3 hours with cooling; washed once with 100 ml of 2 percent HCl solution, and twice with water; dried over magnesium sulfate and concentrated in vacuo in a warm water bath. The resultant solid was recrystallized from 150 ml of ethyl alcohol:water (1:1) with filtering through diatomaceous earth. Collection of the white solid and drying at room temperature in vacuo gave 16.20 g (79.9 percent of theory) of N-methyl-4-methacryloyloxybenzenesulfonamide; m.p.=106° to 107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04335254 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-18cb54244dab4e20a339265cd200cee2 |
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| Source note | uspto-grants-1982_06 |
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