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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 515861생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/515861

반응식

참여 물질

역할이름HCID투입량
반응물2-MethylquinolineHCID 7060—
반응물TriethylamineHCID 8471—
반응물Prolinamide, D-HCID 447554—
반응물Triethylammonium formateHCID 11084032—
촉매Iridium trichlorideHCID 25563—
촉매HCID 178477776HCID 178477776—
용매DichloromethaneHCID 6344—
생성물2-Methyl-1,2,3,4-tetrahydroquinolineHCID 9628967.4%

반응 단계

To 10 ml of methylene chloride, 55.6 mg of a pentamethylcyclopentadienyl iridium(III) chloride dimer ([Cp*IrCl2]2), 16.7 mg of (R)-prolinamide and 15.6 mg of triethylamine were added, and the mixture was stirred under argon atmosphere at room temperature for about 30 minutes to give a catalyst-containing mixture. In 60 ml of methylene chloride, 1.00 g of 2-methylquinoline was dissolved, and a 1/10 amount of the catalyst-containing mixture (equivalent to 0.1 mol % as an iridium chloride dimer) was added. After cooling to −10° C., 8.4 ml of a mixed solvent of formic acid/triethylamine (molar ratio: 5/2) was added dropwise, and the mixture was stirred at the same temperature for 2 days to give 2-methyl-1,2,3,4-tetrahydroquinoline (degree of conversion: 67.4%). The R-enantiomer was in excess and the optical purity was 85.4% ee.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09108986B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-575810ee10444fc9bf54261a52ea2d01
출처 메모uspto-grants-2015_08