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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrifluoroacetic acidHCID 6422—
EduktSodium HydroxideHCID 14798—
EduktMethanedione--ethanol (1/1)HCID 19604758—
Edukt5-carboxymethyl-3-methyl-1H-pyrrole-2,4-dicarboxylic acid 2-tert-butyl ester 4-ethyl esterHCID 49840327—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-carboxymethyl-4-methyl-1H-pyrrole-3-carboxylic acid ethyl esterHCID 4984032885,7%

Reaktionsbedingungen

Temperatur-30 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08697692B2
Quelldatensatzuspto-grants-2014_04
ORD IDord-5451ed90209942a4af7c6e68b96e54c4
Quellennotizuspto-grants-2014_04