돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1801105생성일: 2026년 10월 27일

Water → 2-(3-Bromo-phenyl)-6-chloro-4-hydroxy-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-8-carboxylic acid methyl ester

https://huagongshe.com/reaction/1801105

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물IsobutyraldehydeHCID 6561—
반응물Ytterbium(3+) trifluoromethanesulfonate--water (1/3/1)HCID 45075687—
반응물2-[(3-Bromo-benzylidene)-amino]-5-chloro-benzoic acid methyl esterHCID 67442575—
용매TetrahydrofuranHCID 8028—
생성물2-(3-Bromo-phenyl)-6-chloro-4-hydroxy-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-8-carboxylic acid methyl esterHCID 6744158499.8%

반응 조건

온도25 °C

반응 단계

To a stirred mixture solution of 2-[(3-bromo-benzylidene)-amino]-5-chloro-benzoic acid methyl ester (39.8 g, 113.2 mmol) and ytterbium(III) triflate hydrate (10.5 g, 16.9 mmol) in dry tetrahydrofuran (100 mL) at 25° C. was added isobutyraldehyde (10.4 mL, 113.2 mmol) and water (2.1 mL, 113.2 mmol) dropwise. The reaction mixture was stirred at 25° C. for 16 h. Then the reaction mixture was concentrated in vacuo and the residue was extracted with ethyl acetate (2×200 mL), washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo to afford 2-(3-bromo-phenyl)-6-chloro-4-hydroxy-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-8-carboxylic acid methyl ester (48 g, quant.) as a light yellow oil which was used for next step without further purification: LC/MS m/e calcd for C19H19BrClNO3 (M+H)+: 425.73, observed: 405.9 & 407.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08344137B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-c9475f9e8b6b4529a2fc9611cb184b76
출처 메모uspto-grants-2013_01