HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335516Generated: October 31, 2026
Trifluoroacetic anhydride → HCID 57552585, compound
https://huagongshe.com/reaction/335516
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Carbamide Peroxide | HCID 31294 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | HCID 57552583 | HCID 57552583 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57552585 | HCID 57552585 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08884025B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-86450efc4b144da38400d2e809b29538 |
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| Source note | uspto-grants-2014_11 |
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