HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Allyloxyimino-2-(2-formamidothiazol-4-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | O-Allylhydroxylamine hydrochloride | HCID 3084724 | — |
| Reactant | (2-Formamido-1,3-thiazol-4-yl)(oxo)acetic acid | HCID 13116693 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Allyloxyimino-2-(2-formamidothiazol-4-yl)acetic acid | HCID 54202552 | 66.1% |
Reaction Steps
To a solution of 2-(2-formamidothiazol-4-yl)glyoxylic acid (30 g.) and sodium bicarbonate (12.6 g.) in water (1300 ml.) was added allyloxyamine hydrochloride (19.8 g.), and the mixture was stirred for 7 hours at ambient temperature at pH 6. To the reaction mixture was added ethyl acetate (500 ml.). After the mixture was adjusted to pH 1.9 with 10% hydrochloric acid, the ethyl acetate layer was separated. The ethyl acetate layer was washed with an aqueous solution of sodium chloride, dried over magnesium sulfate and then the solvent was distilled off. The residue was pulverized in diisopropyl ether, collected by filtration and then dried to give 2-allyloxyimino-2-(2-formamidothiazol-4-yl)acetic acid (syn isomer) (25.3 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04304770 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-f364c7c71f074cd1999036250d394703 |
| Source note | uspto-grants-1981_12 |