Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1261511생성일: 2026년 10월 25일
Lithium hydroxide, monohydrate → (S)-4-methyl-2-(1-oxo-4-trifluoromethyl-1,3-dihydro-isoindol-2-yl)-pentanoic acid
https://huagongshe.com/reaction/1261511
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Lithium hydroxide, monohydrate | HCID 168937 | — |
| 반응물 | (S)-4-methyl-2-(1-oxo-4-trifluoromethyl-1,3-dihydro-isoindol-2-yl)-pentanoic acid methyl ester | HCID 70944914 | — |
| 용매 | Oxolane--water (1/1) | HCID 21881883 | — |
| 생성물 | (S)-4-methyl-2-(1-oxo-4-trifluoromethyl-1,3-dihydro-isoindol-2-yl)-pentanoic acid | HCID 70945056 | 97.1% |
반응 단계
A solution of (S)-4-methyl-2-(1-oxo-4-trifluoromethyl-1,3-dihydro-isoindol-2-yl)-pentanoic acid methyl ester (274 mg, 0.83 mmol) in tetrahydrofuran/water (12 mL, 1:1) was treated with lithium hydroxide monohydrate (70 mg, 1.66 mmol) at room temperature. The reaction mixture was then stirred at room temperature for 2 h. After this time, the reaction mixture was concentrated in vacuo to remove the tetrahydrofuran. The resulting material was then diluted with a 1N aqueous hydrochloric acid solution (10 mL) and then extracted with ethyl acetate. The organic layers were combined and then dried over magnesium sulfate, filtered to remove the drying agent, and the filtrate was concentrated in vacuo to afford (S)-4-methyl-2-(1-oxo-4-trifluoromethyl-1,3-dihydro-isoindol-2-yl)-pentanoic acid (254 mg, 97%) as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08470866B2 |
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| 출처 데이터셋 | uspto-grants-2013_06 |
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| ORD ID | ord-48d24c90addf41639db9a50fa56404ab |
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| 출처 메모 | uspto-grants-2013_06 |
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