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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10129생성일: 2026년 10월 24일

Pyridine → (S)-6-benzoyloxy-3-oxo-5-hydroxyhexanoic acid tert-butylester

https://huagongshe.com/ko/reaction/10129

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Benzoyl chlorideHCID 7412—
반응물Sodium HydroxideHCID 14798—
반응물(5S)-5,6-dihydroxy-3-oxohexanoic tert-butyl esterHCID 11401693—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물(S)-6-benzoyloxy-3-oxo-5-hydroxyhexanoic acid tert-butylesterHCID 1509984978%

반응 조건

온도0 °C

반응 단계

To a solution of 16.8 g (77 mmol) of the (5S)-5,6-dihydroxy-3-oxohexanoic tert-butyl ester produced in Example 1 in 120 mL of methylene chloride were added 11.2 mL of pyridine and 10.2 mL of benzoyl chloride at 0° C., and the mixture was stirred at 0° C. for 2 hours. After completion of the reaction, the reaction mixture was diluted with 38 mL of water and adjusted to pH 7 with 20% aqueous NaOH solution. The aqueous layer was separated and further extracted with 2 portions of methylene chloride, 120 mL each. The organic layers were combined and dehydrated over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure to give an oil. This residue was purified by silica gel column chromatography (Kieselgel 60, product of Merck; hexane:acetone=5:1) to give 19.3 g of (5S)-6-benzoyloxy-5-hydroxy-3-oxohexanoic tert-butyl ester (white solid).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094594B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-29050331286246aa9b5102f1f43d720f
출처 메모uspto-grants-2006_08