HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673546Generated: October 25, 2026
Hydrochloric Acid → 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoic acid
https://huagongshe.com/reaction/1673546
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-butyl 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoate | HCID 67344178 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoic acid | HCID 57879346 | 86% |
Reaction Steps
1.0 mL of methanol and 0.5 mL of 2.0 mol/L aqueous sodium hydroxide were added to 1.0 mL of dioxane solution containing 20 mg of tert-butyl 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoate at room temperature and stirred at 50° C. for 30 minutes. Ethyl acetate and 1.0 mol/L hydrochloric acid were added after the reaction mixture was cooled to room temperature. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with a saturated sodium chloride aqueous solution, and the solvent was evaporated under reduced pressure, Diisopropyl ether were added to toe obtained residue and a solid substance was separated by filtration to obtain 15 mg of 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoic acid as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07999132B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-42cbf5a0ad8f41e8942a4333a253c2b3 |
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| Source note | uspto-grants-2011_08 |
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