HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815598Generated: October 29, 2026
Hydrochloric Acid → 2-(2-Aminothiazole-4-yl)-2-acetoxyiminoacetic acid
https://huagongshe.com/reaction/1815598
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 74087995 | HCID 74087995 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Aminothiazole-4-yl)-2-acetoxyiminoacetic acid | HCID 53394825 | 103.9% |
Reaction Steps
2-(2-aminothiazole-4-yl)-2-hydroxyiminoacetate sodium dihydrate (syn-isomer) (24.6 g) was added to water (160 ml) and stirred at 20 to 30° C. Acetic anhydride (28.7 g) was added dropwise thereto for 60 minutes. During the dropwise addition, the pH of the mixture was controlled to 6.0±0.2 by using 20% aqueous sodium carbonate. After the dropwise addition, the mixture was stirred for 30 minutes, and the pH of the mixture was adjusted to 2.5 by using 6N hydrochloric acid. After the reaction liquid was cooled to 5° C., the precipitated crystal was filtered and washed with isopropanol and acetone successively. The obtained wet crystal was dried under reduced pressure to obtain 2-(2-aminothiazole-4-yl)-2-acetoxyiminoacetic acid (syn-isomer) (23.9 g) including two molecules of crystal water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06878827B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-b860408e1a044d9e9d83586e030fd2bf |
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| Source note | uspto-grants-2005_04 |
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