HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → Ethyl 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Ethyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetate | HCID 54525939 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetate | HCID 54209614 | 82.9% |
Reaction Steps
A solution of ethyl 2-(2-tritylaminothiazol-4-yl)-2-allyloxyiminoacetate (syn isomer, 8.7 g), 50% formic acid (42.5 ml) and tetrahydrofuran (42.5 ml) was stirred at 60° C. for 40 minutes. After concentrating the resultant solution in vacuo, the residue was dissolved in ethyl acetate, washed with an aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride in turn, and dried over magnesium sulfate. After concentrating the resultant solution in vacuo, the residue was subjected to column chromatography on silica gel with benzene and ethyl acetate in turn, to give ethyl 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetate (syn isomer, 3.7 g), mp. 102° to 104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04220761 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-d14356388db74f24bf1b93ce184f6b67 |
| Source note | uspto-grants-1980_09 |