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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-Chloromethylsulfinyl-7-fluoro-1-methyl-4-quinoloneHCID 10468547—
SolventDichloromethaneHCID 6344—
Product3-Chloromethylsulfonyl-7-fluoro-1-methyl-4-quinoloneHCID 1010825277.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06730790B2
Source datasetuspto-grants-2004_05
ORD IDord-bcf1ff0b08f74bc88d6d319221187850
Source noteuspto-grants-2004_05