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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Water | HCID 962 | — |
| 반응물 | Isobutyraldehyde | HCID 6561 | — |
| 반응물 | Ytterbium(3+) trifluoromethanesulfonate--water (1/3/1) | HCID 45075687 | — |
| 반응물 | 2-[(3-Bromo-benzylidene)-amino]-5-chloro-benzoic acid methyl ester | HCID 67442575 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(3-Bromo-phenyl)-6-chloro-4-hydroxy-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-8-carboxylic acid methyl ester | HCID 67441584 | 99.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08344137B2 |
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| 출처 데이터셋 | uspto-grants-2013_01 |
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| ORD ID | ord-c9475f9e8b6b4529a2fc9611cb184b76 |
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| 출처 메모 | uspto-grants-2013_01 |
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