HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325380Generated: October 27, 2026
Hydrochloric Acid → 2-(2-Formylamino-5-chlorothiazol-4-yl)-2-oxoacetic Acid
https://huagongshe.com/reaction/325380
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl (2-formamido-5-chlorothiazol-4-yl)glyoxylate | HCID 14326717 | — |
| Reactant | HCID 178473048 | HCID 178473048 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 2-(2-Formylamino-5-chlorothiazol-4-yl)-2-oxoacetic Acid | HCID 19790221 | — |
Reaction Steps
Ethyl 2-(2-formylamino-5-chloro-1,3-thiazol-4-yl)glyoxylate, which can be represented as ethyl 2-(2-formylimino-5-chloro-2,3-dihydro-1,3-thiazol-4-yl)glyoxylate, (1.3 g.) was dissolved in 1 N potassium hydroxide aqueous solution (10 ml.) at room temperature with stirring and the solution was stirred for 5 minutes at the same temperature. After the reaction, the reaction mixture was cooled with ice and then adjusted to pH 1 with 10% hydrochloric acid. The precipitates were collected by filtration, washed with water and then dried to give 2-(2-formylamino-5-chloro-1,3-thiazol-4-yl)glyoxylic acid (0.91 g.), which can be represented as 2-(2-formylimino-5-chloro-2,3-dihydro-1,3-thiazol-4-yl)glyoxylic acid, mp. 148° to 152° C. (dec.). The remaining filtrate and washing were combined together and then extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and then the solvent was distilled off to give further the same object compound (0.23 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04440766 |
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| Source dataset | uspto-grants-1984_04 |
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| ORD ID | ord-f6ffc0b85d694da8aba82b46d5b35d00 |
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| Source note | uspto-grants-1984_04 |
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