HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 515858Erstellt: 26. Oktober 2026
2-Methylquinoline → 2-Methyl-1,2,3,4-tetrahydroquinoline
https://huagongshe.com/reaction/515858
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Methylquinoline | HCID 7060 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Triethylammonium formate | HCID 11084032 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 2-Methyl-1,2,3,4-tetrahydroquinoline | HCID 96289 | 102,1% |
Reaktionsschritte
In 60 ml of methylene chloride, 1.00 g of 2-methylquinoline was dissolved, and 66.5 mg (2.0 mol %) of crystalline (S)-chloro[(1,2,3,4,5-η)-pentamethyl-2,4-cyclopentadien-1-yl](2-pyrrolidinecarboxamidato-κN1, κN2)iridium(III) (Cp*Ir(Cl−)(S-PA-H+)) was added. After cooling to −20° C., 8.4 ml of a mixed solvent of formic acid/triethylamine (molar ratio: 5/2) was added dropwise, and the mixture was continuously stirred at the same temperature for 20 hours. Then, the reaction was completed. The reaction mixture was basified with an aqueous potassium carbonate solution and then the resulting layers were separated. The organic layer was washed with water and concentrated to give 1.05 g of 2-methyl-1,2,3,4-tetrahydroquinoline as an oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09108986B2 |
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| Quelldatensatz | uspto-grants-2015_08 |
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| ORD ID | ord-c7b32f9d35df4118b14194b627fb80da |
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| Quellennotiz | uspto-grants-2015_08 |
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