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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393168Generated: November 2, 2026

16576-25-3 → HCID 54321678, compound

https://huagongshe.com/reaction/2393168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant16576-25-3HCID 727029—
Reactant(5-Carboxypentyl)triphenylphosphanium bromideHCID 2779280—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 54321678HCID 5432167815.8%

Reaction Steps

To a solution of 2-benzoylquinoline (4.0 g) and (5-carboxy-l-pentyl)triphenylphosphonium bromide (11.8 g) in DMSO (50 ml) was added potassium t-butoxide (5.8 g) gradually and the mixture was stirred at room temperature for 30 minutes. This reaction mixture was poured in iced water and washed with toluene. The aqueous layer was neutralized with 3N HCl and extracted with ethyl acetate. The extract was washed with saturated aqueous sodium chloride solution and dried and the solvent was distilled off. The crude residue was purified by silica gel column chromatography (hexane-ethyl acetate=2:1) to give 0.90 g of 7-phenyl-7-(2-quinolyl)-6-heptenoic acid as a mixture of its (E) and (Z) forms. This mixture (0.90 g) and 5% palladium-on-carbon (0.90 g) were suspended in methanol (10 ml) and stirred in a hydrogen atmosphere at room temperature for 3 hours. The catalyst was then filtered off and the filtrate was concentrated to provide the title compound (1.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05804601
Source datasetuspto-grants-1998_09
ORD IDord-ebe3346bd6bc4184b5f1d0fd7a70c8ff
Source noteuspto-grants-1998_09