HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 2-(2-Aminothiazol-4-yl)-2-allyloxyiminoacetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetate | HCID 54209614 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(2-Aminothiazol-4-yl)-2-allyloxyiminoacetic acid | HCID 54484253 | 59.6% |
Reaction Steps
A solution of ethyl 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetate (syn isomer, 3.6 g.), 2N aqueous solution of sodium hydroxide (14.1 ml.), tetrahydrofuran (14.1 ml.) and methanol (15 ml.) was stirred at 40° C. for 1.5 hours. The resultant solution was concentrated in vacuo, and the residue was dissolved in water. After the solution was adjusted to pH 2.8 with 10% hydrochloric acid under ice cooling, the precipitates were collected by filtration, washed with water and acetone in turn and dried to give 2-(2-aminothiazol-4-yl)-2-allyloxyiminoacetic acid (syn isomer, 1.91 g.), mp. 187° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04604456 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-05ef4a3a23484991ac7677f79ecd60a8 |
| Source note | uspto-grants-1986_08 |