Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1770644Generated: November 2, 2026

Sodium Thiosulfate → HCID 178423543, compound

https://huagongshe.com/reaction/1770644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-methyl-N-(thietan-3-yl)-4-[(5S)-5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]benzamideHCID 86727019—
SolventDichloromethaneHCID 6344—
ProductHCID 178423543HCID 178423543—

Reaction Steps

To a suspension of 2-methyl-N-(thietan-3-yl)-4-[(5S)-5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4H-isoxazol-3-yl]benzamide in dichloromethane (92 mL) was added m-CPBA (24.3 mmol, 5.58 g) portion wise at 0-5° C., and the reaction mixture was stirred for 10 min. A saturated Na2S2O3 solution was added, and the mixture was stirred for 10 min. The organic layer was washed with sat. NaHCO3 solution, water and brine, dried over MgSO4, filtered and evaporated. Purification over silica gel (eluent: CH2Cl2/EtOAc) yielded the title compound. LCMS (Method GR) 1.13 min, M+ 539/541; 1H NMR (400 MHz, CDCl3) 2.50 (s, 3H), 3.28 (m, 1H), 3.70 (d, 1H), 4.10-4.20 (m, 4H), 4.70 (m, 1H), 6.50 (d, 1H), 7.40-7.70 (1d+4s, 5H), 19F-NMR (CDCl3, 376 MHz): −79.43. Chiral HPLC Method Column: Daicel CHIRALPAK® IB, 3 μm, 0.46 cm×10 cm Mobile phase: Heptan/EtOH 80/20 Retention times of eluting isomers: 4.85 min (8.2%) 5.66 min (91.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09247740B2
Source datasetuspto-grants-2016_02
ORD IDord-0b0f37b3cfa840b0b6affb6e966be600
Source noteuspto-grants-2016_02