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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

반응식

참여 물질

역할이름HCID투입량
반응물2-Ketobutyric acid methyl esterHCID 545127—
반응물Oxolane--water (1/1)HCID 21881883—
반응물3-(1,3-Dioxolan-2-yl)-2-fluoro-4-iodopyridineHCID 22744998—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물Methyl 2-[3-(1,3-dioxolan-2-yl)-2-fluoro-4-pyridinyl]-2-hydroxybutanoateHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06699876B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-9eab1e4ca5d14b6daf542e4f10225a96
출처 메모uspto-grants-2004_03