HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropyl Ether → 2-(2-Formamidothiazol-4-yl)-2-(2-formyloxyethoxyimino)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-(2-Aminothiazol-4-yl)-2-(2-hydroxyethoxyimino)acetic acid | HCID 54403470 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 2-(2-Formamidothiazol-4-yl)-2-(2-formyloxyethoxyimino)acetic acid | HCID 54133317 | — |
Reaction Steps
A solution of formic acid (1.6 g.) and acetic anhydride (3.6 g.) was stirred at 50° C. for an hour. After cooling, 2-(2-aminothiazol-4-yl)-2-(2-hydroxyethoxyimino)acetic acid (syn isomer, 1 g.) was added to the solution and stirred at room temperature for 3 hours. Diisopropyl ether was added to the resultant solution, and the precipitates were filtered out. The filtrate was concentrated in vacuo, and the residue was pulverized with diisopropyl ether. The precipitates were collected by filtration to give 2-(2-formamidothiazol-4-yl)-2-(2-formyloxyethoxyimino)acetic acid (syn isomer, 0.7 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04220761 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-e1cd387611074e05a33c963b553c4fba |
| Source note | uspto-grants-1980_09 |