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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 461260생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/461260

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 93) in 85 ml. 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 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 0.5N 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, λ maxMeOH. = 220 mμ (7450); ν max - 1715 (carbonyl groups) and 1095 cm-1 (methoxy group).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04061672
출처 데이터셋uspto-grants-1977_12
ORD IDord-ef54f193d2174bdeab23677e56e0f83d
출처 메모uspto-grants-1977_12