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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
Reactant1-(4-Fluoro-2-methylaminophenyl)-2-methylsulphonylethanoneHCID 54037846—
SolventChloroformHCID 6212—
Product5'-fluoro-N-methyl-2'-methylsulphonylacetylformanilideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05079264
Source datasetuspto-grants-1992_01
ORD IDord-ece9edd46e3e4dbfac707b4e4a56472a
Source noteuspto-grants-1992_01