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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323165Generated: October 25, 2026

(4-Carboxybutyl)triphenylphosphonium bromide → 4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(5-carboxy-1-pentenyl)phenyl]benzamide

https://huagongshe.com/reaction/323165

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Carboxybutyl)triphenylphosphonium bromideHCID 161236—
Reactant4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-formylphenyl)benzamideHCID 22010987—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
Product4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(5-carboxy-1-pentenyl)phenyl]benzamideHCID 7006873167.7%

Reaction Steps

To an ice bath cooled solution of (4-carboxybutyl)triphenylphosphonium bromide (371 mg) in N,N-dimethylacetamide (15 ml) was added potassium t-butoxide (188 mg) and the mixture was stirred at the same temperature for 30 minutes. To the resulting mixture was added 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-formylphenyl)benzamide (250 mg) and the mixture was stirred in an ice bath for 3 hours. The mixture was diluted with ethyl acetate (40 ml) and the solution was washed successively with 1N hydrochloric acid (30 ml), water (20 ml) and brine (20 ml). The organic phase was dried over magnesium sulfate and the solvent was evaporated in vacuo to give an oil. The crude oil was purified by silica gel column (1% methanol in chloroform) to give 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(5-carboxypenten-1-yl)phenyl]benzamide (201 mg) as a colorless amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211242B1
Source datasetuspto-grants-2001_04
ORD IDord-8da00f1b70e04d54a83cc5747f0c5e8c
Source noteuspto-grants-2001_04