HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2364980Erstellt: 25. Oktober 2026
Trifluoroacetic acid → 2-carboxymethyl-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester
https://huagongshe.com/reaction/2364980
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Methanedione--ethanol (1/1) | HCID 19604758 | — |
| Edukt | 5-carboxymethyl-3-methyl-1H-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl ester | HCID 49840327 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-carboxymethyl-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester | HCID 49840328 | 85,7% |
Reaktionsschritte
A solution of 5-carboxymethyl-3-methyl-1H-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl ester (6.3 g, 20 mmol) in 600 ml of dichloromethane and trifluoroacetic acid (120 ml, 1.55 mol) was heated to reflux under a nitrogen atmosphere for 2.5 hours. The reaction mixture was stirred in the dry ice-ethanol bath and added with aqueous sodium hydroxide solution (1.55 mol sodium hydroxide in 100 ml of water) while maintaining the temperature at −30° C. Upon completion of the addition, the mixture was extracted with dichloromethane (100 ml×7). The combined organic extracts were washed with brine (100 ml), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give 2-carboxymethyl-4-methyl-1H-pyrrole-3-carboxylic acid ethyl ester (3.6 g, 85.7%) as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08697692B2 |
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| Quelldatensatz | uspto-grants-2014_04 |
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| ORD ID | ord-5451ed90209942a4af7c6e68b96e54c4 |
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| Quellennotiz | uspto-grants-2014_04 |
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