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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-(2-Aminothiazol-4yl)-2-n-butoxyiminoacetic acid | HCID 54024302 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 2-(2-Formamidothiazol-4-yl)-2-butoxyiminoacetic acid | HCID 54132484 | 72.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04400379 |
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| Source dataset | uspto-grants-1983_08 |
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| ORD ID | ord-84c8665ddf4345c29f53ad05f61d35bf |
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| Source note | uspto-grants-1983_08 |
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