Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantSodium IodideHCID 5238—
ReactantTriphenylphosphineHCID 11776—
ReactantBenzhydryl 7-salicylideneamino-3-chloromethyl-3-cephem-4-carboxylateHCID 136460599—
SolventDimethylformamideHCID 6228—
ProductBenzhydryl 7-salicylideneamino-3-vinyl-3-cephem-4-carboxylateHCID 13646059278.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04487927
Source datasetuspto-grants-1984_12
ORD IDord-2a52e1c16ec74457b8a80bf58a16eae6
Source noteuspto-grants-1984_12