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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 249153Generated: October 29, 2026

Hydrochloric Acid → HCID 19024724, compound

https://huagongshe.com/reaction/249153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIndoleHCID 798—
ReactantHCID 19024785HCID 19024785—
ReactantHCID 178418573HCID 178418573—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 19024724HCID 1902472416.9%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of indole (366 mg) in tetrahydrofuran (5 ml) was added 3M solution of methyl magnesium bromide in ether (1.5 ml) at 20° C., and the mixture was stirred at 20° C. for 1 hour. A solution of 4-[2,2-bis(4-isobutylphenyl)ethyl]benzoyl chloride (450 mg) in tetrahydrofuran (5 ml) was added to the mixture at 20° C. After stirred at 20° C. for 30 minutes, the mixture was poured into a mixture of 1N hydrochloric acid and ethyl acetate. The organic layer was separated, washed with water, aqueous sodium bicarbonate and brine, and dried over magnesium sulfate. After evaporation of the solvent, the residue was purified by column chromatography on silica gel (10 g) eluting with a mixture of hexane and ethyl acetate (20:1) to give 3-[4-[2,2-bis(4-isobutylphenyl)ethyl]benzoyl]indole (90 mg) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212320
Source datasetuspto-grants-1993_05
ORD IDord-cc1a803bd5c8427db54ee748d1228f40
Source noteuspto-grants-1993_05