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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720068Generated: November 1, 2026

Hydrochloric Acid → HCID 22419955, compound

https://huagongshe.com/reaction/1720068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 2-methylacetoacetateHCID 701—
ReactantPotassium HydroxideHCID 14797—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(2-Phenylethyl)aniline--hydrogen chloride (1/1)HCID 22419956—
ReactantSodium NitriteHCID 23668193—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 22419955HCID 22419955—

Reaction Steps

Solid NaNO2 (0.35 g, 5 mmol) was added to a suspension of the p-phenethylaniline hydrochloride (1.1 g, 5 mmol) and concentrated HCl (2 ml) in H2O (3 ml) under an icewater bath. The solution was kept at -5° C. with stirring while ethyl 2-methylacetoacetate (0.72 g, 5 mmol)in EtOH 95% (5 ml) was treated at -10° C. with a solution of 50% KOH (1.7 ml) followed at once by ice (10 g). The diazo-solution was then added immediately, stirred at room temperature for 20 min, and extracted with Et2O (2×20 ml). The combined Et2O portions were dried (MgSO4) and the solvent was removed under reduced pressure to give a red oil which was taken up in anhydrous EtOH (10 ml), and dry hydrogen chloride gas was passed through the solution until ammonium chloride was precipitated. The mixture was heated at reflux for 20 min, and then stirred at room temperature for 2 h. The suspension was poured into ice water (100 ml) and extracted with Et2O (2×30 ml). The combined Et2O portions were dried (MgSO4) and the solvent was removed under reduced pressure to give a solid which was recrystallized from EtOH 95% to provide 3-ethyloxycarbonyl-5-(2-phenylethyl)indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05504101
Source datasetuspto-grants-1996_04
ORD IDord-c17aa2d6fc814f1f929304cb1ce040e6
Source noteuspto-grants-1996_04