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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28470생성일: 2026년 10월 24일

Water → (2s)-1-(Benzyloxy)-3-[(5-bromo-2-methyl-6-quinolinyl)oxy]-2-propanol

https://huagongshe.com/ko/reaction/28470

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물(-)-Benzyl (R)-glycidyl etherHCID 159746—
반응물5-Bromo-2-methylquinolin-6-olHCID 11230138—
용매DimethylacetamideHCID 31374—
생성물(2s)-1-(Benzyloxy)-3-[(5-bromo-2-methyl-6-quinolinyl)oxy]-2-propanolHCID 1136163873%

반응 단계

A solution of 5-bromo-2-methyl-6-quinolinol (30.1 g, 126 mmol), (R)-benzyl glycidyl ether (24.9 g, 152 mmol) and triethylamine (17.4 g, 172 mmol) in DMA (200 mL) was heated in a 95-98° C. oil bath for 2 days. The solution was cooled and poured into water (300 mL) while stirring. The tan precipitate formed was filtered, washed with water (100 mL) and dried in a vacuum oven to give 37 g (73%) of the title compound as a tan solid. Rf=0.35 (EtOAc); 1H NMR (DMSO) δ 8.31 (d, J=8.8 Hz, 1H), 7.96 (d, J=9.2 Hz, 1H), 7.72 (d, J=9.3 Hz, 1H), 7.74 (d, J=8.7 Hz, 1H), 7.25-7.36 (m, 5H), 5.28 (d, J=5.1 Hz, 1H), 4.56 (s, 2H), 4.22-4.29 (m, 2H), 4.08-4.15 (m, 1H), 3.61-3.73 (m, 2H), 2.66 (s, 3H); Specific rotation=+6.2° (c=1, CH3OH);

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419986B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-397c5821208849d79fa594c5c5fe3a84
출처 메모uspto-grants-2008_09