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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 374825Generated: October 30, 2026

Water → 6-(3-Acetylaminophenyl)-6-(3-pyridyl)hex-5-enoic acid

https://huagongshe.com/reaction/374825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(4-Carboxybutyl)triphenylphosphonium bromideHCID 161236—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 53837382HCID 53837382—
SolventTetrahydrofuranHCID 8028—
Product6-(3-Acetylaminophenyl)-6-(3-pyridyl)hex-5-enoic acidHCID 53792000—

Reaction Steps

To a mixture of 217 g of 4-carboxybutyl-triphenylphosphonium bromide and 154 g of potassium tert.butoxide in 1.8 liters of tetrahydrofuran are added, at -25° C., 94 g of 3-acetylaminophenyl-3-pyridyl ketone. After 2 hours stirring at ambient temperature the reaction mixture is combined with 200 ml of water and then substantially evaporated down. The residue is taken up in 500 ml of water and washed with ethyl acetate. The aqueous phase is then neutralised by the addition of citric acid and extracted with ethyl acetate. The organic phase is evaporated down and the residue is recrystallised from ethyl acetate/acetone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05482948
Source datasetuspto-grants-1996_01
ORD IDord-0bc1f5315ad34ca48e606dd262ce8542
Source noteuspto-grants-1996_01