Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 13564037 | HCID 13564037 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13472284 | HCID 13472284 | — |
Reaction Steps
A solution of 0.625 g. of p-nitrobenzyl 7β-(2-thienylacetamido)-3-azido-3-cephem-4-carboxylate in 24 ml. of THF was diluted with 10 ml. of cold water and cooled in an ice-water bath. To the cold solution were added portionwise over about two hours 1.58 g. of zinc dust and sufficient 0.1N to 1N hydrochloric acid to maintain the pH of the mixture at about 4.3. Throughout the addition of zinc and acid the temperature of the reaction mixture was maintained at about 5° C. After the zinc dust addition was completed, the pH was adjusted to 2.7 with 1N hydrochloric acid and the mixture filtered. The filtrate was mixed with ethyl acetate and extracted twice with aqueous sodium bicarbonate. The aqueous layer was separated, layered with ethyl acetate, acidified with cold 1N hydrochloric acid, the organic layer separated, washed with brine, dried, and evaporated to yield 0.116 g. of the title acid as a pale yellow solid. The product was triturated with diethyl ether, filtered, and air dried to provide 80 mg. of the product acid as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04521598 |
|---|
| Source dataset | uspto-grants-1985_06 |
|---|
| ORD ID | ord-46ff5f7ea7924891a5dd59664f11c6bf |
|---|
| Source note | uspto-grants-1985_06 |
|---|