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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1627383Erstellt: 26. Oktober 2026

Acetic Acid → N'-(3,5-difluoro-4-formylphenylsulfonyl)-N,N-dimethylformimidamide

https://huagongshe.com/reaction/1627383

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktDimethylformamideHCID 6228—
EduktLithium diisopropylamideHCID 2724682—
EduktN'-(3,5-difluorophenylsulfonyl)-N,N-dimethylformimidamideHCID 66740661—
KatalysatorDiisopropylamineHCID 7912—
KatalysatorButyllithiumHCID 178418339—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN'-(3,5-difluoro-4-formylphenylsulfonyl)-N,N-dimethylformimidamideHCID 8666225779,7%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of diisopropylamine (231 mL, 1.63 mmol, 2.1 eq) in THF (1 L) was slowly added BuLi (2.5M in Hex, 653 mL, 1.63 mmol, 2.1 eq) at 0° C. The solution was cooled to −78° C., and then a solution of N′-(3,5-difluorophenylsulfonyl)-N,N-dimethylformimidamide (193 g, 777 mmol) in THF (1 L) was added dropwise to the stirred LDA solution over 1 h at −78° C. and allowed to stir another 2 h at same temperature. To the reaction mixture was added anhyd DMF (72 mL, 932 mmol, 1.2 eq) and, 30 minutes later, was added AcOH (50 mL) and water. The reaction mixture was extracted with EtOAc (500 mL×3). The combined extracts were washed with brine (1 L), dried over MgSO4 and concentrated in vacuo to give N′-(3,5-difluoro-4-formylphenylsulfonyl)-N,N-dimethylformimidamide (171 g), which was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08785488B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-84346d24da954764b26d0e688f43621a
Quellennotizuspto-grants-2014_07