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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507907Generated: October 30, 2026

2-Methylbenzenesulfonic acid → HCID 178469953, compound

https://huagongshe.com/reaction/1507907

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylbenzenesulfonic acidHCID 6925—
ReactantEthyl (2E)-3-ethoxy-2-propenoateHCID 5366269—
ReactantSodium t-butoxideHCID 23676156—
ReactantMethyl 1-amino-4-fluoro-1H-pyrrole-2-carboxylateHCID 66985030—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 178469953HCID 17846995353.3%

Reaction Conditions

Temperature85 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221826B2
Source datasetuspto-grants-2015_12
ORD IDord-52e787401c424ebe9af5928c19bd9de9
Source noteuspto-grants-2015_12