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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-[3-(3-Hydroxybenzoyl)indol-1-yl]butyric acid | HCID 19024708 | — |
| Reactant | HCID 19101766 | HCID 19101766 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[3-[3-[Bis(4-isobutylphenyl)methoxy]benzoyl]indol-1-yl]butyric acid | HCID 19024772 | 12.9% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05212320 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-1f22e7be4adb48989a6f57358ff78c52 |
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| Source note | uspto-grants-1993_05 |
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