Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1869153생성일: 2026년 10월 26일
Lithium hydroxide, monohydrate → 1-(2-(Trifluoromethyl)quinolin-4-yl)-1H-indole-3-carboxylic acid
https://huagongshe.com/reaction/1869153
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Lithium hydroxide, monohydrate | HCID 168937 | — |
| 반응물 | 3-methoxycarbonyl-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indole | HCID 68970592 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-(2-(Trifluoromethyl)quinolin-4-yl)-1H-indole-3-carboxylic acid | HCID 68972955 | — |
반응 단계
0.204 g (4.9 mmol) of lithium hydroxide monohydrate and 8 cm3 of water are added to 0.6 g (1.62 mmol) of 3-methoxycarbonyl-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indole dissolved in 8 cm3 of tetrahydrofuran. After stirring at reflux for 15 hours, the reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa) to give a residue which is taken up in 20 cm3 of water (pH=10). The resulting aqueous solution is washed with 30 cm3 of ethyl acetate, adjusted to pH 6 with N hydrochloric acid and extracted with 50 cm3 of ethyl acetate. The organic phase is dried over magnesium sulphate and concentrated to dryness under reduced pressure (2.7 kPa). The solid obtained is triturated in 20 cm3 of isopropyl ether and filtered off, resulting in 0.3 g of 3-carboxy-1-(2-(trifluoromethyl)quinol-4-yl)-1H-indole in the form of a yellow powder. Mass spectrum (EI): m/e 356 (M+•), m/e 311.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07638521B2 |
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| 출처 데이터셋 | uspto-grants-2009_12 |
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| ORD ID | ord-d37b4a9f20ea4fc38641b5986370be79 |
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| 출처 메모 | uspto-grants-2009_12 |
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