HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Cyclohexanedione → 3-(4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Cyclohexanedione | HCID 10434 | — |
| Reactant | Aminolevulinic Acid Hydrochloride | HCID 123608 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-oxo-4,5,6,7-tetrahydro-1H-indol-3-yl)propanoic acid | HCID 15832721 | 82% |
Reaction Conditions
| Temperature | 110 °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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06531502B1 |
| Source dataset | uspto-grants-2003_03 |
| ORD ID | ord-259b9799725f44119a12c5d96fa5459e |
| Source note | uspto-grants-2003_03 |