HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070372Generated: October 31, 2026
Hydrochloric Acid → N-Methacryloyl-5-aminosalicylic acid
https://huagongshe.com/reaction/1070372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 5-Aminosalicylic Acid | HCID 4075 | — |
| Reactant | Methacrylic Acid | HCID 4093 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-Methacryloyl-5-aminosalicylic acid | HCID 171252 | 74.5% |
Reaction Steps
Into a 1 liter flask were added 600 ml of acetonitrile, 95.2 g (1.1 mol) of methacrylic acid and 120.1 g (1.1 mol) of chloroformic acid ethyl ester. To this mixture 111.8 g (1.1 mol) of triethylamine was added over a period of 1 hour in a cold bath. Stirring was continued for 1 hour at room temperature and 141.2 g (1 mol) of 5-aminosalicylic acid was added. The mixture was heated for 2 hours at 60° C. The mixture was poured into 5 liter of 1% HCl solution. The deposit was filtered, washed and dried to produce 164.7 g of N-(3-carboxy-4-hydroxyphenyl)methacrylamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06902860B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-951222f37f934a7984e42aff27eff827 |
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| Source note | uspto-grants-2005_06 |
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