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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670736Generated: October 25, 2026

Hydrochloric Acid → 7-Fluoro-2,3,4,9-tetrahydro-1H-beta-carboline

https://huagongshe.com/reaction/1670736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant2-(6-fluoro-1H-indol-3-yl)ethanamineHCID 854024—
ReactantHydrogen chloride-ethyl acetateHCID 21866389—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product7-Fluoro-2,3,4,9-tetrahydro-1H-beta-carbolineHCID 1507755068%

Reaction Steps

6-Fluorotryptamine (0.71 g) was dissolved in tetrahydrofuran (30 ml), a 4N hydrochloric acid-ethyl acetate solution (1.2 ml) was added dropwise, and the mixture was stirred at room temperature. The solvent was evaporated under reduced pressure. Glyoxylic acid monohydrate (Aldrich Co., 403 mg), a 1N potassium hydroxide solution (3.98 ml) and water (80 ml) were added to the obtained residue, and the mixture was stirred with heating at 80° C. for 1.5 hr. After ice-cooling, the precipitate was collected by filtration and washed with water to give a pale-brown solid. Water (80 ml) and concentrated hydrochloric acid (2 ml) were added to the obtained solid, and the mixture was stirred with heating at 80° C. for 1 hr. Concentrated hydrochloric acid (2 ml) was further added, and the mixture was heated under reflux for 1 hr. The insoluble material was hot filtrated, and the filtrate was adjusted to pH 12 or above with a 6N aqueous sodium hydroxide solution. The precipitated solid was collected by filtration, washed with water, and dried to give 7-fluoro-2,3,4,9-tetrahydro-1H-β-carboline (516 mg, yield 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994196B2
Source datasetuspto-grants-2011_08
ORD IDord-c10ca2faf9eb499c9614850ab2a3a47a
Source noteuspto-grants-2011_08