HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetate → HCID 70352943, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetate | HCID 84468 | — |
| Reactant | HCID 70582096 | HCID 70582096 | — |
| Solvent | Anisole | HCID 7519 | — |
| Product | HCID 70352943 | HCID 70352943 | 73.8% |
Reaction Steps
To a suspension of 0.443 g of the 7-amino-3-thiadiazole benzyhydryl ester obtained in Example 78 in 2 ml of anisole is added 3 ml of trifluoroacetate acid under stirring and ice-cooling. After 30 minutes, the solvent is distilled off under reduced pressure. The residue is dissolved in 10% hydrochloric acid and the solution is neutralized with a saturated aqueous solution of sodium bicarbonate. The formed precipitates are filtered, and washed with water, acetone and then ether to give 0.21 g of 7-amino-3-(5-methyl-1,3,4-thiadiazol-2-yl)-3-cephem-4-carboxylic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04182866 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-a4ccf762d8e846a4b3a2b3074741a5cb |
| Source note | uspto-grants-1980_01 |