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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225351생성일: 2026년 10월 26일

Methanol → 7-(3-Methoxy-5-oxocyclopent-1-EN-1-YL)heptanoic acid

https://huagongshe.com/reaction/225351

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물2,6-LutidineHCID 7937—
반응물4-Bromo-2-(6-carboxyhexyl)cyclopent-2-en-1-oneHCID 13046277—
촉매Silver tetrafluoroborateHCID 159722—
생성물7-(3-Methoxy-5-oxocyclopent-1-EN-1-YL)heptanoic acidHCID 23330004—

반응 단계

To a stirred solution of 5.30 g. of crude 4-bromo-2-(6-carboxyhexyl)cyclopent-2-en-1-one (Example 8) in 85ml. of methanol at 0°-3° C. is added 4.40 g. (22.6 mmole) of silver fluoborate in one portion. After 2 minutes, the mixture is treated with 2.66 g. (24.8 l mmoles) of 2,6-lutidine. After stirring for 30 minutes at 0°-3° C. the mixture is stirred at ambient temperature for 45 minutes. Silver bromide is removed by filtration, and the filtrate is concentrated to a volume of 40 ml. The solution is treated with saturated sodium chloride solution and extracted with ether. The extract is washed successively with 0.5 N hydrochloric acid solution, water, and saturated sodium chloride solution; dried over magnesium sulfate; and concentrated. Partition chromatography of the residue on Celite gives an oil, λmax.MeOH =220 mμ (7450); νmax.=1715 (carbonyl groups) and 1095 cm-1 (methoxy group).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04236027
출처 데이터셋uspto-grants-1980_11
ORD IDord-9964a853461340b797a30370fb59136b
출처 메모uspto-grants-1980_11