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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917344Generated: October 31, 2026

Sodium Sulfite → 5-Benzyloxy-3-methylsulfinyl-1,2,4-thiadiazole

https://huagongshe.com/reaction/917344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant5-Benzyloxy-3-methylthio-1,2,4-thiadiazoleHCID 11708511—
SolventChloroformHCID 6212—
Product5-Benzyloxy-3-methylsulfinyl-1,2,4-thiadiazoleHCID 23032447—

Reaction Steps

Into 12 ml of chloroform was dissolved 1.39 g of 5-benzyloxy-3-methylthio-1,2,4-thiadiazole, and metachloroperbenzoic acid (>70%) was slowly added to the mixture under ice-cooling. After stirring for 1 hour, the compound of low-polarity from the reaction mixture was detected by thin layer chromatography. The reaction mixture was poured into a saturated sodium sulfite aqueous solution, and separated. The organic layer was washed with sodium hydrogen carbonate aqueous solution, dried over anhydrous sodium sulfate, concentrated to give 1.4 g of 5-benzyloxy-3-methylsulfinyl-1,2,4-thiadiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273879B2
Source datasetuspto-grants-2007_09
ORD IDord-04ca18a34702406382ef4ef7c318ef5d
Source noteuspto-grants-2007_09