HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 2-(2-Aminothiazol-4-yl)-2-(2,4-dichlorobenzyloxyimino)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 1-Methylimidazole | HCID 1390 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ethyl 2-(2-aminothiazol-4-yl)-2-(2,4-dichlorobenzyloxyimino)acetate | HCID 54440018 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-(2-Aminothiazol-4-yl)-2-(2,4-dichlorobenzyloxyimino)acetic acid | HCID 54076453 | 90.1% |
Reaction Steps
A solution of 1-methylimidazole (0.5 g.) in 1 N sodium hydroxide aqueous solution (48 ml.) was added to a solution of ethyl 2-(2-aminothiazol-4-yl)-2-(2,4-dichorobenzyloxyimino)acetate (syn isomer, 12.0 g.), methanol (120 ml.) and tetrahydrofuran (100 ml.) at 15° to 20° C., and stirred at 35° to 40° C. for 6 hours. After removing methanol and tetrahydrofuran in vacuo from the resultant mixture, the aqueous residue was washed with ethyl acetate. Ethyl acetate was completely removed from the aqueous solution and adjusted to pH 2.0 with hydrochloric acid. The precipitates were collected by filtration to give 2-(2-aminothiazol-4-yl)-2-(2,4-dichlorobenzyloxyimino)acetic acid (syn isomer, 10.0 g.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04372952 |
| Source dataset | uspto-grants-1983_02 |
| ORD ID | ord-24a7d1cce7594c86839bb70031a79d3b |
| Source note | uspto-grants-1983_02 |