Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656159Generated: November 1, 2026

Triphenylphosphine → HCID 131713156, compound

https://huagongshe.com/reaction/1656159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 131713158HCID 131713158—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 131713156HCID 13171315649.9%

Reaction Steps

To a solution of benzhydryl 7-[2-(2-formamidothiazol-4-yl)-2-methoxyiminoacetamido]-3-chloromethyl-3-cephem-4-carboxylate (syn isomer) (25.0 g) in ethyl acetate (300 ml) was added a solution of triphenylphosphine (21.0 g) in tetrahydrofuran (170 ml), and the mixture was heated under reflux for 10 hours. The precipitated substance was collected by filtration to give [7-(2-(2formamidothiazol-4-yl)-2-methoxyiminoacetamido)-4-benzhydryloxycarbonyl-3-cephem-3-yl]methyl-triphenylphosphonium chloride (syn isomer) (17.7 g). The remained filtrate was heated under reflux for 10 hours. Similarly, the precipitated substance was collected by filtration to recover the same product (9.75 g). Further, this operation was repeated once to recover the same product (3.3 g). Total yield: 30.75 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252731
Source datasetuspto-grants-1993_10
ORD IDord-0a9c346a66184678ad5fa3d2dd6cb4a2
Source noteuspto-grants-1993_10