HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700430Generated: October 31, 2026
1-Amino-2-propanol → 3-Methyl-6-(2-methylphenyl)-4,5,6,7-tetrahydroindol-4-one
https://huagongshe.com/reaction/1700430
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Amino-2-propanol | HCID 4 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 1,3-Cyclohexanedione, 5-phenyl- | HCID 568962 | — |
| Product | 3-Methyl-6-(2-methylphenyl)-4,5,6,7-tetrahydroindol-4-one | HCID 11107440 | — |
Reaction Steps
A mixture of 5-phenylcyclohexane-1,3-dione (2.0 g), 3-aminopropan-2-ol (0.97 g), molecular sieves 4A (12 g) and tetrahydrofuran (30 ml) was refluxed for 12 hours and cooled, and insoluble materials were filtered off. Under reduced pressure, the solvent was evaporated, and the residue was dissolved in dimethylformamide (40 ml). To the mixture were added 2-bromomesitylene (2.0 g), tetrakistriphenylphosphine palladium (0.29 g) and potassium carbonate (2.7 g), and the mixture was stirred at 150° C. for 5 hours and concentrated under reduced pressure. The residue was dissolved in ethyl acetate, and the solution was washed with sodium hydrogen carbonate solution, water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-hexane to give colorless crystals of 3-methyl-6-(2-methylphenyl)-4,5,6,7-tetrahydroindol-4-one (1.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06350749B1 |
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| Source dataset | uspto-grants-2002_02 |
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| ORD ID | ord-792fe49068e84f7b86d04dedfffa125c |
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| Source note | uspto-grants-2002_02 |
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