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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917342Generated: October 30, 2026

Acetic Anhydride → 5-Bezyloxy-3-acetoxymethythio-1,2,4-thiadiazole

https://huagongshe.com/reaction/917342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2,6-LutidineHCID 7937—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Benzyloxy-3-methylsulfinyl-1,2,4-thiadiazoleHCID 23032447—
Product5-Bezyloxy-3-acetoxymethythio-1,2,4-thiadiazoleHCID 5896289464.5%

Reaction Steps

Into 1.5 g of acetic anhydride were added 620 mg of 2,6-lutidine and 500 mg of 5-benzyloxy-3-methylsulfinyl-1,2,4-thiadiazole under ice-cooling. After stirring for 15 hours at room temperature, the reaction mixture was added to saturated sodium hydrogen carbonate aqueous solution, and extracted with t-butyl methyl ether. The organic layer was concentrated, and the residue obtained was subjected to silica gel column chromatography to give 376 mg of 5-bezyloxy-3-acetoxymethythio-1,2,4-thiadiazole (hereinafter, referred to as the present compound (44)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273879B2
Source datasetuspto-grants-2007_09
ORD IDord-54c407c5d82d447f93314033ab40fc69
Source noteuspto-grants-2007_09