HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089774Generated: October 25, 2026
Formic Acid → 5'-fluoro-N-methyl-2'-methylsulphonylacetylformanilide
https://huagongshe.com/reaction/1089774
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-(4-Fluoro-2-methylaminophenyl)-2-methylsulphonylethanone | HCID 54037846 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 5'-fluoro-N-methyl-2'-methylsulphonylacetylformanilide | HCID 86744742 | — |
Reaction Steps
A mixture of acetic anhydride (19.8 ml) and formic acid (13.5 ml) was stirred and heated at 60° under nitrogen for 2 hours. 1-(4-Fluoro-2-methylaminophenyl)-2-methylsulphonylethanone (10.0 g), was added portionwise to the mixture at ambient temperature with stirring. The mixture was stirred at 30° for 30 minutes. Water (30 ml) was added to the reaction mixture which was then stirred at 30° for 30 minutes. Concentration of the reaction mixture by evaporation in vacuo gave a green oil. The oil was dissolved in trichloromethane (50 ml) and washed with aqueous sodium hydrogen carbonate solution (7% w/w; 2×30 ml). The trichloromethane extract was dried (magnesium sulphate) and evaporated in vacuo to give a green oil which solidified at ambient temperature. Recrystallisation from toluene gave 5'-fluoro-N-methyl-2'-methylsulphonylacetylformanilide, m.p. 94.5°-95.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05079264 |
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| Source dataset | uspto-grants-1992_01 |
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| ORD ID | ord-ece9edd46e3e4dbfac707b4e4a56472a |
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| Source note | uspto-grants-1992_01 |
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