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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 72238Erstellt: 24. Oktober 2026

Diisopropylamine → 5-Formyl-3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/de/reaction/72238

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
Edukt1-PiperidinecarboxaldehydeHCID 17429—
EduktAmmonium ChlorideHCID 25517—
EduktMethyl 3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylateHCID 2805185—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt5-Formyl-3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl esterHCID 57618725—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A 1.6M n-BuLi solution in hexane (12 mL) was added dropwise to a solution of diisopropylamine (2.9 mL) in THF (30 mL) at −78° C. The reaction mixture was stirred at 0° C. for 10 min and then cooled to −78° C., and a solution of 3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl ester (1.5 g) in THF (15 mL) was added. The reaction mixture was stirred at −78° C. for 30 min and then 1-formylpiperidine (4 g) was added, and the mixture was again stirred at this temperature for 1.5 h. Subsequently, saturated ammonium chloride solution was added and the reaction mixture was allowed to reach room temperature. The aqueous phase was extracted several times with ethyl acetate. The combined organic phases were dried over sodium sulfate and the solvent was removed in vacuo. The product with the molecular weight of 281.0 (C9H6F3NO4S) was obtained in this way; MS (ESI): 282 (M+H+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08828991B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-063af6f49cc04f6fbaaa08dfff6a4a13
Quellennotizuspto-grants-2014_09