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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylamine | HCID 7912 | — |
| Edukt | 1-Piperidinecarboxaldehyde | HCID 17429 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Methyl 3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylate | HCID 2805185 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 5-Formyl-3-(2,2,2-trifluoroacetylamino)thiophene-2-carboxylic acid methyl ester | HCID 57618725 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08828991B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-063af6f49cc04f6fbaaa08dfff6a4a13 |
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| Quellennotiz | uspto-grants-2014_09 |
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