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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335516Generated: October 31, 2026

Trifluoroacetic anhydride → HCID 57552585, compound

https://huagongshe.com/reaction/335516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantCarbamide PeroxideHCID 31294—
ReactantSodium BisulfiteHCID 23665763—
ReactantHCID 57552583HCID 57552583—
SolventWaterHCID 962—
ProductHCID 57552585HCID 57552585—

Reaction Conditions

Temperature0 °C

Reaction Steps

The 3-Methoxycarbonyloxy-5-methylsulfanyl-isothiazole-4-carboxylic acid methyl ester slurry was cooled to 0° C., and urea hydrogen peroxide addition compound (2.8 equiv, 12.8 g) was added. Trifluoroacetic acid anhydride (2.8 equiv, 19.2 mL, 28.4 g) was added dropwise over 20 minutes. The mixture stirred at 0° C. for 45 minutes, and quenched with sodium hydrogen sulfite (2.0 equiv, 10.0 g) in water (90 mL, 9 volumes) and stirred at 25° C. Most of the acetonitrile was removed under vacuum, then the aqueous residue was extracted once with 100 mL and once again with 50 mL dichloromethane to provide 5-Methanesulfonyl-3-methoxycarbonyloxy-isothiazole-4-carboxylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08884025B2
Source datasetuspto-grants-2014_11
ORD IDord-86450efc4b144da38400d2e809b29538
Source noteuspto-grants-2014_11