HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854196Generated: October 30, 2026
Methanol → 5-Formyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylic Acid
https://huagongshe.com/reaction/854196
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 5-formyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester | HCID 20604779 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Formyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylic Acid | HCID 21915619 | 52% |
Reaction Steps
5-Formyl-2-methyl-4-phenyl-1H-pyrrole-3-carboxylic acid ethyl ester was dissolved in water (100 mL) and methanol (45 mL) with stirring. Added KOH (2 eq. 1.9 g) and heated in 100° C. After 2.5 h, cooled to room temperature and the remaining ester was removed by extracting into ethyl acetate (200 mL), dried and concentrated. The water layer was acidified to pH=3 using 2N HCl. The white solid was removed by filtration, rinsing with water. The solid was re-concentrated from toluene, triturated with hexanes and dried to afford 2 g (52%) of an off-white solid. 1H NMR (360 MHz, DMSO-d6) δ 12.46 (br s, 1H, CO2H), 11.95 (s, 1H, NH), 9.08 (s, 1H, CHO), 7.36 (s, 5H, ArH), 2.49 (s, 3H, CH3). MS m/z (relative intensity %, ion) found 229 (100, M+); calc. 229.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07256189B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-17ed10cb51dd4b4a9d081bc48b67f66f |
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| Source note | uspto-grants-2007_08 |
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