HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Benzhydryl 7-salicylideneamino-3-hydroxymethyl-3-cephem-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | HCID 136460587 | HCID 136460587 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Benzhydryl 7-salicylideneamino-3-hydroxymethyl-3-cephem-4-carboxylate | HCID 136460596 | 91.3% |
Reaction Steps
To a suspension of 7-salicylideneamino-3-hydroxymethyl-3-cephem-4-carboxylic acid dicyclohexylamine salt (3 g) in ethyl acetate (60 ml) was added dropwise an ethyl acetate solution of p-toluenesulfonic acid (1.1 g) with stirring, and the reaction mixture was stirred for an hour at ambient temperature. After the precipitate was filtered off, the filtrate was treated with a solution of excess diphenyldiazomethane in ethyl acetate for an hour. The solvent was distilled off, and the residue was pulverized with diisopropyl ether, collected by filtration and dried to give benzhydryl 7-salicylideneamino-3-hydroxymethyl-3-cephem-4-carboxylate (2.66 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04423213 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-8cb93efd4eaf4a50a25b783014da18a2 |
| Source note | uspto-grants-1983_12 |