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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1440836Generated: October 25, 2026

Hydrochloric Acid → 1H-Indole-3-ethanamine, 7-chloro-

https://huagongshe.com/reaction/1440836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-Chlorophenylhydrazine hydrochlorideHCID 443287—
Reactant2-(4,4-Diethoxybutyl)isoindoline-1,3-dioneHCID 12805186—
SolventEthanolHCID 702—
Product1H-Indole-3-ethanamine, 7-chloro-HCID 145709—

Reaction Steps

A 10.0 g sample of 2-chlorophenylhydrazine hydrochloride and 17.9 g of 4-phthalimidobutyraldehyde diethyl acetal were stirred in 200 mL ethanol with 1 mL 5N HCl. The mixture was concentrated to a residue which was slurried in a small amount of methylene chloride. A yellow solid was collected and vacuum dried at 40° C. The solid was stirred in 500 mL ethanol. Hydrazine hydrate (14 g) was added and the mixture was heated at reflux for 14 hours. A 60 mL sample of 5N HCl was added and the mixture was heated at reflux for 1 hour. The mixture was allowed to cool and was concentrated to a residue. The residue was partitioned between 1N NaOH and chloroform. The organic layer was separated and the aqueous layer was extracted with chloroform. The combined extracts were dried (Na2SO4) and concentrated to an oil. The oil was chromatographed on silica gel using a gradient of 0-10% methanol in chloroform containing 0.2% ammonium hydroxide. Fractions containing product were concentrated to an oil which was taken up in a small amount of methanol and added to ethereal HCl. A solid was collected, washed with diethyl ether, and vacuum dried at 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05500431
Source datasetuspto-grants-1996_03
ORD IDord-2ffdad1e8a4149f399eaa8d73265f33d
Source noteuspto-grants-1996_03