HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 5-formyl-4-methyl-1H-pyrrole-2-carboxylic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 5-formyl-4-methyl-1H-pyrrole-2-carboxylate | HCID 9855648 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-formyl-4-methyl-1H-pyrrole-2-carboxylic Acid | HCID 9898884 | 99.4% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a solution of 0.8 g (4.4 mmol) of 5-formyl-4-methyl-1H-pyrrole-2-carboxylic acid ethyl ester in 35 mL of water and 15 mL of ethanol was added 0.5 g (8.9 mmol) of potassium hydroxide. The reaction mixture was heated to 100° C. for 1 hour, cooled to room temperature, and evaporated ethanol. The water layer was acidified to pH=3 using 2N. hydrogen chloride solution. The precipitate was filtered and washed with water to afford 0.67 g (68%) of 5-formyl-4-methyl-1H-pyrrole-2-carboxylic acid as a tan solid. 1H NMR (360 MHz, DMSO-d6) δ12.92 (br s, 1H, CO2H), 12.48 (br s, 1H, NH), 9.76 (s, 1H, CHO-5), 6.63 (s, 1H), 2.28 (s, 3H, CH3). MS m/z 152 [M−1].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06908930B2 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-cb70ee2a989c4ae08d06223303976c00 |
| Source note | uspto-grants-2005_06 |