Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20488생성일: 2026년 10월 25일
Lithium hydroxide, monohydrate → 3-((1S)-2-{[tert-Butyl(dimethyl)silyl]oxy}-1-methylethoxy)-5-[4-(methylsulfonyl)phenoxy]benzoic acid
https://huagongshe.com/reaction/20488
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Lithium hydroxide, monohydrate | HCID 168937 | — |
| 반응물 | methyl 3-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-5-[4-(methylsulfonyl)phenoxy]benzoate | HCID 59346872 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-((1S)-2-{[tert-Butyl(dimethyl)silyl]oxy}-1-methylethoxy)-5-[4-(methylsulfonyl)phenoxy]benzoic acid | HCID 59346907 | 71% |
반응 단계
Lithium hydroxide monohydrate (346 mg, 8.24 mmol) was added to a solution of methyl 3-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-5-[4-(methylsulfonyl)phenoxy]benzoate (3.70 g, 7.49 mmol) in THF (50 mL) and water (10 mL) and the reaction stirred for 2 h. A further portion of lithium hydroxide monohydrate (346 mg, 8.24 mmol) was then added and the reaction was heated at 45° C. for 1.5 h. The THF was then evaporated and water layer was extracted with diethyl ether (10 mL). The remaining aqueous layer was acidified with 5% w/v aqueous citric acid and extracted (2×50 mL) with ethyl acetate and the combined organic layers were dried (MgSO4), filtered and evaporated to afford the title compound as a gum (2.54 g, 71%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07745475B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-4a82ea0189664ddbbbe2d51f548d35ac |
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| 출처 메모 | uspto-grants-2010_06 |
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