HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Ethoxyimino-2-(5-formamido-1,2,4-thiadiazol-3-yl)acetic acid | HCID 53759301 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetic acid | HCID 54350992 | 75% |
Reaction Steps
A mixture of 2-ethoxyimino-2-(5-formamido-1,2,4-thiadiazol-3-yl)acetic acid (syn isomer) (4.4 g) and 1 N aqueous solution of sodium hydroxide (54 ml) was stirred for 2 hours at 50° to 55° C. The mixture was cooled in an ice bath, acidified with hydrochloric acid (5.4 ml) and extracred with ethyl acetate. The extract was dried over magnesium sulfate and evaporated to dryness. The residue was triturated with diethyl ether to give 2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetic acid (syn isomer) (2.92 g), mp. 168° to 170° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04447429 |
| Source dataset | uspto-grants-1984_05 |
| ORD ID | ord-6b9a6bec9429434fb92086ca724621eb |
| Source note | uspto-grants-1984_05 |