HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089773Generated: October 25, 2026
m-Chloroperbenzoic acid → 1-(4-Fluoro-2-methylaminophenyl)-2-methylsulphonylethanone
https://huagongshe.com/reaction/1089773
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethanone, 1-[4-fluoro-2-(methylamino)phenyl]-2-(methylsulfinyl)- | HCID 10059700 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Fluoro-2-methylaminophenyl)-2-methylsulphonylethanone | HCID 54037846 | — |
Reaction Steps
A solution of 3-chloroperoxybenzoic acid (8.29 g) in dichloromethane (200 ml) was added to a solution of 1-(4-fluoro-2-methylaminophenyl)-2-methylsulphinylethanone (10.0 g), prepared in a similar manner to that described in Example 1, in dichloromethane (175 ml) over a period of 7 minutes whilst maintaining the temperature below 30°. The mixture was stirred at ambient temperature for 2 hours, saturated aqueous sodium hydrogen carbonate solution (244 ml) was added and the mixture stirred at ambient temperature for a further 2 hours. The dichloromethane layer was isolated and the aqueous layer extracted with dichloromethane (2×60 ml). The organic phases were combined, dried (magnesium sulphate) and evaporated in vacuo to give a solid which was crystallised from acetone to give 1-(4-fluoro-2-methylaminophenyl)-2-methylsulphonylethanone, m.p. 143.5°-145°.
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-4415c8cfc16b463cb1e2dd733ac71a4b |
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| Source note | uspto-grants-1992_01 |
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