HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372387Generated: November 1, 2026
Potassium Hydroxide → HCID 21071878, compound
https://huagongshe.com/reaction/1372387
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 14840866 | HCID 14840866 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21071878 | HCID 21071878 | 40% |
Reaction Steps
4-Carboxymethyl-3,5-dimethyl-1H-pyrrole-2-carboxylic acid wet mixture (778 g, 3.95 mol), 880 mL of 9 N potassium hydroxide and 880 mL of water were heated to an internal temperature of 65° C., removed from the heat, and 800 mL of 10 N hydrochloric acid were slowly added with stirring to a pH of 2.5. The temperature increased to 68° C. and then decreased to 58° C. with the evolution of carbon dioxide. Thin layer chromatography (ethyl acetate:hexane:acetic acid 4:6:0.5) showed a major spot at Rf 0.7 and a small spot at the origin. The mixture was cooled to 4° C. The solids were collected by vacuum filtration and washed 3 times with 200 mL of water each time. The solid was air dried to give 240 g (40% yield) of (2,4-dimethyl-1H-pyrrol-3-yl)-acetic acid as a brown solid. 1H-NMR (dimethylsulfoxide-d6) δ 1.89, 2.06 (2×s, 2×3H, 2×CH3), 3.17 (s, 2H, CH2), 6.26 (s, 1H, pyrrole CH), 10.02 (s, 1H, NH), 11.74 (br s, 1H, COOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157577B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-0838d9d6cb764b13a52f1f020194babc |
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| Source note | uspto-grants-2007_01 |
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