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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947216Generated: November 4, 2026

Sodium Thiosulfate → HCID 59829848, compound

https://huagongshe.com/reaction/1947216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59829798HCID 59829798—
SolventDichloromethaneHCID 6344—
ProductHCID 59829848HCID 5982984879%

Reaction Steps

While stirring in ice cold conditions, 3-chloroperbenzoic acid (4.20 g, 24.4 mmol) was added to a methylene chloride (10 mL) solution of 4-isopropyl-3-(5-isopropyl-2,4-bis-methoxymethoxyphenyl)-5-methylsulfanyl-4H-[1,2,4]triazole (F63-04, 1.93 g, 4.87 mmol). After stirring at room temperature for 2 hours, the mixture was bring back to ice cold conditions again, and saturated aqueous sodium thiosulfate and then saturated aqueous sodium hydrogencarbonate were added. After stirring for a while, the reaction mixture was extracted with ethyl acetate, and the extract was washed with saturated sodium chloride solution. After drying the extract over anhydrous sodium, sodium sulfate was removed by filtration and the solvent was distilled off under reduced pressure to obtain a pale yellow foam. After purification by silica gel column chromatography (hexane, ethyl acetate), 4-isopropyl-3-(5-isopropyl-2,4-bis-methoxymethoxyphenyl)-5-methylsulfonyl-4H-[1,2,4]triazole (F63-05, colorless foam, 1.65 g, 79%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399464B2
Source datasetuspto-grants-2013_03
ORD IDord-4968977727da4271869e66f1097c2479
Source noteuspto-grants-2013_03