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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249168Generated: October 30, 2026

Hydrochloric Acid → 4-[3-[3-[Bis(4-isobutylphenyl)methoxy]benzoyl]indol-1-yl]butyric acid

https://huagongshe.com/reaction/249168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactant4-[3-(3-Hydroxybenzoyl)indol-1-yl]butyric acidHCID 19024708—
ReactantHCID 19101766HCID 19101766—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product4-[3-[3-[Bis(4-isobutylphenyl)methoxy]benzoyl]indol-1-yl]butyric acidHCID 1902477212.9%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 4-[3-(3-hydroxybenzoyl)indol-1-yl]butyric acid (500 mg) in N,N-dimethylformamide (5 ml) was added to a suspension of sodium hydride (60% dispersion in mineral oil, 136 mg) in N,N-dimethylformamide (10 ml) at 25° . The mixture was stirred at 25° C. for 1 hour, and a solution of bis (4-isobutylphenyl)bromomethane (1.11 g) in tetrahydrofuran (10 ml) was added at 0° C. After stirred at 25° C. overnight, the mixture was poured into a mixture of ethyl acetate and 1N hydrochloric acid. The organic layer was separated, washed with water and brine, and dried over magnesium sulfate. After evaporation of the solvent, the residue was chromatographed on silica gel (20 g) eluting with 2% methanol in chloroform to give 4-[3-[3-[bis(4-isobutylphenyl)methoxy]benzoyl]indol-1-yl]butyric acid (120 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212320
Source datasetuspto-grants-1993_05
ORD IDord-1f22e7be4adb48989a6f57358ff78c52
Source noteuspto-grants-1993_05