HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089769Generated: October 25, 2026
Formic Acid → 5'-fluoro-N-methyl-2'-methylsulphinylacetylformanilide
https://huagongshe.com/reaction/1089769
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethanone, 1-[4-fluoro-2-(methylamino)phenyl]-2-(methylsulfinyl)- | HCID 10059700 | — |
| Product | 5'-fluoro-N-methyl-2'-methylsulphinylacetylformanilide | HCID 86744741 | — |
Reaction Steps
A mixture of acetic anhydride (16.5 ml) and formic acid (11.2 ml) was stirred and heated at 50°-60° under nitrogen for 2 hours. The mixture was cooled to just below 0° and 1-(4-fluoro-2-methylaminophenyl)-2-methylsulphinylethanone (17.2 g), prepared in a similar manner to that described in Example 1, added over a period of 5 minutes. The mixture was stirred at just below 0° for 5 hours and then stored at 4° overnight. The mixture was cooled in an ice/salt bath to maintain the temperature below 0° whilst water (60 ml) was added. The mixture was evaporated in vacuo below 15° to give a green/brown oil. Purification of the oil by high performance liquid chromatography carried out using a Gilson system fitted with a 2" Dynamax silica column and eluting with dichloromethane/methanol (97.5:2.5) at 20 ml/min gave 5'-fluoro-N-methyl-2'-methylsulphinylacetylformanilide in the form of a colourless oil.
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-98b3ff8a3b674120bf649ccf1c84812c |
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| Source note | uspto-grants-1992_01 |
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