HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28282Generated: October 25, 2026
Acetic Anhydride → Ethyl 2-(formylamino)-alpha-oxo-4-thiazoleacetate
https://huagongshe.com/reaction/28282
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | Ethyl 2-formamidothiazol-4-acetate | HCID 688091 | — |
| Reactant | HCID 178470762 | HCID 178470762 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethyl 2-(formylamino)-alpha-oxo-4-thiazoleacetate | HCID 2733245 | — |
Reaction Steps
A mixture of manganous acetate tetrahydrate (120 g.), acetic acid (1000 ml) and acetic anhydride (100 ml.) was stirred for 20 minutes in an oil bath heated at 130° to 135° C., and to the mixture was added potassium permanganate (20 g.) over 5 minutes at 105° to 110° C. with stirring and then the mixture was further stirred for 30 minutes at 130° to 135° C. The mixture was cooled to room temperature, and to the mixture was added ethyl 2-(2-formylaminothiazol-4-yl)acetate, which can be represented as ethyl 2-(2-formylimino-2,3-dihydrothiazol-4-yl)acetate, (53.5 g.), and then the mixture was stirred for 15 hours at 38° to 40° C. under introduction of air at the rate of 6000 ml. per minute. After the reaction, the precipitates were collected by filtration. The precipitates were washed with acetic acid and water in turn and then dried to give ethyl 2-(2-formylaminothiazol-4-yl)glyoxylate, which can be represented as ethyl 2-(2-formylimino-2,3-dihydrothiazol-4-yl)glyoxylate, (41.5 g.), mp 232° to 233° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04225707 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-7ccb5fd1af4b433096c4032ff4abacd9 |
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| Source note | uspto-grants-1980_09 |
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