Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 47357생성일: 2026년 10월 24일
2-Ketobutyric acid methyl ester → Methyl 2-[3-(1,3-dioxolan-2-yl)-2-fluoro-4-pyridinyl]-2-hydroxybutanoate
https://huagongshe.com/ko/reaction/47357
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Ketobutyric acid methyl ester | HCID 545127 | — |
| 반응물 | Oxolane--water (1/1) | HCID 21881883 | — |
| 반응물 | 3-(1,3-Dioxolan-2-yl)-2-fluoro-4-iodopyridine | HCID 22744998 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | Methyl 2-[3-(1,3-dioxolan-2-yl)-2-fluoro-4-pyridinyl]-2-hydroxybutanoate | HCID 22745040 | — |
반응 단계
6.9 ml (11 mmol) of 1.6M butyllithium in hexane are added dropwise to a solution, stirred at −78° C. under an argon atmosphere, of 3.1 g (11 mmol) of 3-(1,3-dioxolan-2-yl)-2-fluoro-4-iodopyridine in 100 ml of THF. The reaction mixture is then stirred for 10 minutes at −78° C. before the dropwise addition of a solution of 1.5 g (13 mmol) of methyl 2-oxo-butyrate in 20 ml of THF. The mixture is stirred for 3 hours at −78° C., hydrolysed with a mixture of water/THF, and decanted. The aqueous phase is extracted 3 times with 50 ml of ethyl acetate each time, and the combined organic phases are dried over magnesium sulphate and then concentrated. The expected product is obtained by purification of the residue by chromatography over silica (eluant: dichloromethane/acetone 95/5).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06699876B2 |
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| 출처 데이터셋 | uspto-grants-2004_03 |
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| ORD ID | ord-9eab1e4ca5d14b6daf542e4f10225a96 |
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| 출처 메모 | uspto-grants-2004_03 |
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