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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83901Generated: October 26, 2026

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

https://huagongshe.com/reaction/83901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDimethylformamideHCID 6228—
ReactantLithium diisopropylamideHCID 2724682—
ReactantN'-(3,5-difluorophenylsulfonyl)-N,N-dimethylformimidamideHCID 66740661—
CatalystDiisopropylamineHCID 7912—
CatalystButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN'-(3,5-difluoro-4-formylphenylsulfonyl)-N,N-dimethylformimidamideHCID 8666225779.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846739B2
Source datasetuspto-grants-2014_09
ORD IDord-ebfce5adf6ee4f9daaee6a438cd85d5d
Source noteuspto-grants-2014_09