HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261850Generated: October 25, 2026
Hydrochloric Acid → 2-(2-Aminothiazole-4-yl)-2-methoxyiminoacetic acid
https://huagongshe.com/reaction/261850
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-(2-aminothiazol-4-yl)-2-methoxyiminoacetate | HCID 581091 | — |
| Reactant | HCID 178472869 | HCID 178472869 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(2-Aminothiazole-4-yl)-2-methoxyiminoacetic acid | HCID 125216 | — |
Reaction Steps
Ethanol (10 ml.) was added to a suspension of ethyl 2-methoxyimino-2-(2-aminothiazol-4-yl)acetate (syn isomer), which can be represented as ethyl 2-methoxyimino-2-(2-imino-2,3-dihydrothiazol-4yl)acetate (syn isomer), (2.2 g.) in a 1N aqueous solution of sodium hydroxide (12 ml.) and the mixture was stirred for 15 hours at ambient temperature. The reaction mixture was adjusted to pH 7.0 with 10% hydrochloric acid and ethanol was distilled off under reduced pressure. The residual aqueous solution was washed with ethyl acetate, adjusted to pH 2.8 with 10% hydrochloric acid and stirred under ice-cooling to precipitate crystals. The crystals were collected by filtration, washed with acetone and recrystallized from ethanol to give colorless needles of 2-methoxyimino-2-(2-aminothiazol-4-yl)acetic acid (syn isomer), which can be represented as 2-methoxyimino-2-(2-imino-2,3-dihydrothiazol-4-yl)acetic acid (syn isomer), (1.1 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04152433 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-c7eb4212d99a48119440e33386823026 |
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| Source note | uspto-grants-1979_05 |
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