HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581769Generated: October 25, 2026
m-Chloroperbenzoic acid → 3-Chloromethylsulfonyl-7-fluoro-1-methyl-4-quinolone
https://huagongshe.com/reaction/1581769
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 3-Chloromethylsulfinyl-7-fluoro-1-methyl-4-quinolone | HCID 10468547 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Chloromethylsulfonyl-7-fluoro-1-methyl-4-quinolone | HCID 10108252 | 77.6% |
Reaction Steps
6.33 g (0.0232 mole) of monochloroflosequinan (4) and 225 ml of methylene dichloride were placed in a 500 ml round bottom flask and stirred. Into this mixture a 5.98 g of 77% pure m-chloroperoxybenzoic acid (8) was added in four equal portions in 15 minute intervals and the mixture was stirred for an additional 30 minutes to complete oxidation. The reaction mixture was then concentrated to a final volume of 100 ml and the crystals which formed were filtered off and washed with two 10 ml portions of methylene dichloride. After high vacuum drying 5.2 g (77.6% yield) of white crystalline 3-chloromethylsulfonyl-7-fluoro-1-methyl-4-quinolone (9) were collected. The product was 99+% pure (by 1H NMR). 1H NMR, CDCl3, δ=8.52 dd, 1H, J=6.3 & 9.0 Hz, H at C5; 8.41 s, 1H, H at C2; 7.20 dd, 1H, J=2.1 & 9.6 Hz, H at C8; 7.32-7.26 m, 1H, H at C6; 5.03 s, 2H, CH2; 3.94 s, 3H, N—CH3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06730790B2 |
|---|
| Source dataset | uspto-grants-2004_05 |
|---|
| ORD ID | ord-bcf1ff0b08f74bc88d6d319221187850 |
|---|
| Source note | uspto-grants-2004_05 |
|---|