HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089768Generated: October 25, 2026
Formic Acid → 5'-fluoro-N-methyl-2'-(methylthio)acetylformanilide
https://huagongshe.com/reaction/1089768
Participants
| Role | Name | HCID | Charge |
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| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 1-(4-Fluoro-2-methylaminophenyl)-2-(methylthio)ethanone | HCID 19978474 | — |
| Product | 5'-fluoro-N-methyl-2'-(methylthio)acetylformanilide | HCID 86744740 | — |
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 ambient temperature and 1-(4-fluoro-2-methylaminophenyl)-2-(methylthio)ethanone (4.0 g), prepared in a similar manner to that described in Example 4, added over a period of 5 minutes. The mixture was stirred at ambient temperature for 2.75 hours and then cooled in an ice/salt bath to maintain the temperature below 30° whilst, water (50 ml) was added over a period of 30 minutes. The mixture was extracted with dichloromethane (2×25 ml), the organic phases combined, washed with water (2×20 ml) and then evaporated in vacuo to give an oily product. Purification of the oily product by high performance liquid chromatography carried out using a Gilson system fitted with a 2" Dynamax silica column and eluting with dichloromethane/methanol (99:1) at 16 ml/min gave 5'-fluoro-N-methyl-2'-(methylthio)acetylformanilide in the form of a pale yellow 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-100ae3f7bb5f4cdf899760d9a6bfa8aa |
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| Source note | uspto-grants-1992_01 |
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