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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24337Generated: October 26, 2026

1,3-Cyclohexanedione → 3-(4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)propanoic acid

https://huagongshe.com/reaction/24337

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-CyclohexanedioneHCID 10434—
ReactantAminolevulinic Acid HydrochlorideHCID 123608—
ReactantSodium AcetateHCID 517045—
SolventWaterHCID 962—
Product3-(4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)propanoic acidHCID 1583272182%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 5-aminolevulinic acid hydrochloride (1.68 g, 10 mmol), 1,3-cyclohexanedione (1.12 g, 10 mmol) and sodium acetate (1.64 g, 20 mmol) in water (10 mL) was stirred at 110° C. for 4 hr and then cooled. The precipitate which formed was collected by vacuum filtration, washed with 30% of ethanol in water and dried under vacuum to give 1.7 g (82%) of 3-(4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)-propionic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855730B2
Source datasetuspto-grants-2005_02
ORD IDord-14c68bff05ad47c583145b78f82585b7
Source noteuspto-grants-2005_02