HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1154196Generated: October 27, 2026
Isopropanol → Benzhydryl 7-salicylideneamino-3-vinyl-3-cephem-4-carboxylate
https://huagongshe.com/reaction/1154196
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzhydryl 7-salicylideneamino-3-chloromethyl-3-cephem-4-carboxylate | HCID 136460599 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzhydryl 7-salicylideneamino-3-vinyl-3-cephem-4-carboxylate | HCID 136460592 | 78.4% |
Reaction Steps
To a cooled solution of benzhydryl 7-salicylideneamino-3-chloromethyl-3-cephem-4-carboxylate (4 g) in dimethylformamide (10 ml) were added triphenylphosphine (2.2 g) and sodium iodide with stirring. After stirring for 2 hours at ambient temperature, the reaction mixture was poured into isopropyl alcohol (250 ml), and the precipitated solids (6.7 g) were collected by filtration. To a stirred solution of the above solids in methylene chloride (10 ml) and water (5 ml) was added 36% formaldehyde solution (17.4 ml). Then the reaction mixture was adjusted to pH 9.0 with a saturated aqueous sodium bicarbonate. After stirring for an hour at ambient temperature, the separated organic layer was washed with water and an aqueous sodium chloride, followed by drying over magnesium sulfate. The solution was evaporated under reduced pressure to give benzhydryl 7-salicylideneamino-3-vinyl-3-cephem-4-carboxylate (3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04487927 |
|---|
| Source dataset | uspto-grants-1984_12 |
|---|
| ORD ID | ord-2a52e1c16ec74457b8a80bf58a16eae6 |
|---|
| Source note | uspto-grants-1984_12 |
|---|