HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Benzhydryl 7-salicylideneamino-3-chloromethyl-3-cephem-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Benzhydryl 7-salicylideneamino-3-hydroxymethyl-3-cephem-4-carboxylate | HCID 136460596 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzhydryl 7-salicylideneamino-3-chloromethyl-3-cephem-4-carboxylate | HCID 136460599 | 85.9% |
Reaction Conditions
| Temperature | -30 °C |
|---|
Reaction Steps
Benzhydryl 7-salicylideneamino-3-hydroxymethyl-3-cephem-4-carboxylate (1.01 g) was dissolved in methylene chloride (10 ml) and cooled to -30° C. To this solution was added phosphorus pentachloride (0.46 g), followed by addition of pyridine (0.18 ml). The reaction mixture was stirred for an hour at -30° to -20° C. and poured into ice-water. The separated organic layer was washed with water and an aqueous sodium chloride, followed by drying over magnesium sulfate. The solvent was evaporated in vacuo to give benzhydryl 7-salicylideneamino-3-chloromethyl-3-cephem-4-carboxylate (0.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05110921 |
| Source dataset | uspto-grants-1992_05 |
| ORD ID | ord-664264bcc197492b927e13d5634f1196 |
| Source note | uspto-grants-1992_05 |