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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 435247Generated: October 29, 2026

Acetic Anhydride → 2-(2-Formamidothiazol-4-yl)-2-butoxyiminoacetic acid

https://huagongshe.com/reaction/435247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2-(2-Aminothiazol-4yl)-2-n-butoxyiminoacetic acidHCID 54024302—
SolventFormic AcidHCID 284—
Product2-(2-Formamidothiazol-4-yl)-2-butoxyiminoacetic acidHCID 5413248472.1%

Reaction Steps

Formic acid (18.95 g.) was added dropwise to acetic anhydride (42.0 g.) under stirring at room temperature over 5 minutes, and stirred at 50° C. for an hour. 2-(2-Aminothiazol-4-yl)-2-n-butoxyiminoacetic acid (syn isomer, 25 g.) was added to the solution under ice cooling, and stirred at room temperature for 3 hours and additionally at 30° C. for an hour. After concentrating the resultant solution in vacuo, the residue was dissolved in diethyl ether. The solution was washed with water and a saturated aqueous solution of sodium chloride in turn, dried over magnesium sulfate and concentrated in vacuo. The obtained oil was triturated with a solution of n-hexane (1 part) and diisopropyl ether (1 part), and collected by filtration to give 2-(2-formamidothiazol-4-yl)-2-n-butoxyiminoacetic acid (syn isomer, 20.1 g.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04400379
Source datasetuspto-grants-1983_08
ORD IDord-84c8665ddf4345c29f53ad05f61d35bf
Source noteuspto-grants-1983_08