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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515858Generated: October 26, 2026

2-Methylquinoline → 2-Methyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/515858

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylquinolineHCID 7060—
ReactantPotassium CarbonateHCID 11430—
ReactantTriethylammonium formateHCID 11084032—
SolventDichloromethaneHCID 6344—
Product2-Methyl-1,2,3,4-tetrahydroquinolineHCID 96289102.1%

Reaction Conditions

Temperature-20 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108986B2
Source datasetuspto-grants-2015_08
ORD IDord-c7b32f9d35df4118b14194b627fb80da
Source noteuspto-grants-2015_08