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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374824Generated: October 31, 2026

(4-Carboxybutyl)triphenylphosphonium bromide → HCID 54557606, compound

https://huagongshe.com/reaction/374824

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Carboxybutyl)triphenylphosphonium bromideHCID 161236—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 67745971HCID 67745971—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54557606HCID 54557606—

Reaction Steps

To a suspension of 307 g of 4-carboxybutyltriphenylphosphonium bromide and 233 g of potassium tert.butoxide in 2.8 liters of tetrahydrofuran are added, at -40° C., 140 g of 4-acetylaminophenyl-3-pyridyl-ketone and this mixture is stirred for 2 hours. The reaction mixture is decomposed by the addition of ice water and evaporated down. The residue is taken up in water and washed with ethyl acetate. The aqueous phase is acidified to pH 5 to 6 and extracted with ethyl acetate. The organic phase is concentrated by evaporation and the residue is recrystallised from ethyl acetate/diisopropylether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482948
Source datasetuspto-grants-1996_01
ORD IDord-b540687b52e4443e827dd1fa1c729479
Source noteuspto-grants-1996_01