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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | N'-(3,5-difluorophenylsulfonyl)-N,N-dimethylformimidamide | HCID 66740661 | — |
| Catalyst | Diisopropylamine | HCID 7912 | — |
| Catalyst | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N'-(3,5-difluoro-4-formylphenylsulfonyl)-N,N-dimethylformimidamide | HCID 86662257 | 79.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846739B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-ebfce5adf6ee4f9daaee6a438cd85d5d |
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| Source note | uspto-grants-2014_09 |
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