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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565964Generated: October 30, 2026

Sodium Thiosulfate → HCID 18472671, compound

https://huagongshe.com/reaction/565964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 18472267HCID 18472267—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18472671HCID 1847267179.9%

Reaction Steps

To a solution of (E)-N-[4-(3-pyridyl)phenyl]-3-(4-methylphenyl)cinnamamide (250 mg) in tetrahydrofuran (20 ml) was added 3-chloroperbenzoic acid (70%, 0.24 g) at 0° C., and the mixture was stirred at room temperature for 18 hours. To the reaction mixture was added sodium thiosulfate solution, and the mixture was stirred for a few minutes and extracted with dichloromethane. The organic layer was washed with saturated sodium bicarbonate solution and saturated sodium chloride solution, dried with magnesium sulfate and concentrated. The residue was recrystallized from ethanol-tetrahydrofuran-acetone to give (E)-N-[4-(1-oxidopyridin-3-yl)phenyl]-3-(4-methylphenyl)-cinnamamide (Compound 193) (208 mg) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06172061B2
Source datasetuspto-grants-2001_01
ORD IDord-ac487f1f46924a63ad6f7865bda1b852
Source noteuspto-grants-2001_01