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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838646Generated: November 1, 2026

Water → HCID 18755515, compound

https://huagongshe.com/reaction/1838646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPeracetic AcidHCID 6585—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 18755535HCID 18755535—
SolventDichloromethaneHCID 6344—
ProductHCID 18755515HCID 1875551584%

Reaction Steps

0.8 g (0.00204 mol) of the 2-(2-methyl-6-trifluoromethylpyridine-3-carbonyl)-3-phenylsulfanylcyclohex-2-enone obtained above is dissolved in 30 ml of methylene chloride, and 1.39 ml of peracetic acid (39% in acetic acid, 0.00816 mol) are subsequently added dropwise at a temperature of 25° C. After 4 hours at 25° C., the reaction mixture is poured into ethyl acetate and water, the organic phase is washed with water, dried with sodium sulfate and concentrated, and the residue is triturated with a small amount of hexane and ethyl acetate. Filtration gives 0.72 g (84% of theory) of 3-benzenesulfonyl-2-(2-methyl-6-trifluoromethyl-pyridine-3-carbonyl)cyclohex-2-enone in the form of white crystals of melting point 165-167° C. 1H-NMR (CDCl3): 2.30, m, 2H; 2.55, t (J, 7 Hz), 2H; 2.71, m, 2H; 3.05, s, 3H; 7.40-7.80, m, 4H; 7.80-8.05 ppm, m, 3H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673938B1
Source datasetuspto-grants-2004_01
ORD IDord-d0feed1da3a04d3ab8436dc6dd009e4d
Source noteuspto-grants-2004_01