HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507907Generated: October 30, 2026
2-Methylbenzenesulfonic acid → HCID 178469953, compound
https://huagongshe.com/reaction/1507907
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methylbenzenesulfonic acid | HCID 6925 | — |
| Reactant | Ethyl (2E)-3-ethoxy-2-propenoate | HCID 5366269 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | Methyl 1-amino-4-fluoro-1H-pyrrole-2-carboxylate | HCID 66985030 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178469953 | HCID 178469953 | 53.3% |
Reaction Steps
A mixture of methyl 1-amino-4-fluoro-1H-pyrrole-2-carboxylate (0.980 g, 6.20 mmol), (E)-ethyl 3-ethoxyacrylate (1.25 g, 8.68 mmol) and toluenesulfonic acid (0.059 g, 0.310 mmol) in ethanol (15 mL) was heated at 85° C. for 2 h then at reflux (100° C. bath) for an additional 2 h. The mixture was cooled and concentrated to remove the ethanol/water and additional ethanol was added and reconcentrated. The process was repeated until all of the water had been removed then residue was dissolved in ethanol (15 mL) and sodium tert-butoxide (1.190 g, 12.39 mmol) was added to make orange clear solution. This mixture was heated at 85° C. for 1 h, then cooled and concentrated to remove the ethanol and the reaction mixture was neutralized with HCl in dioxane (0.5 mL of 4N solution) then concentrated to afford a tan semi solid. This material was slurried in water and stirred for 1 h and the resulting solid was collected and rinsed with water and filtered and dried to afford the title compound (740 mg, 3.30 mmol, 53.3% yield) as a light yellow solid. HPLC (condition B): retention time=3.57 min. LCMS (condition B): m/z 224.9 +ve.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221826B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-52e787401c424ebe9af5928c19bd9de9 |
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| Source note | uspto-grants-2015_12 |
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