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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 473952생성일: 2026년 10월 25일

3-Oxo-cyclopentanecarboxylic acid methyl ester → Cyclopentanecarboxylic acid, 3-hydroxy-, methyl ester

https://huagongshe.com/reaction/473952

반응식

참여 물질

역할이름HCID투입량
반응물3-Oxo-cyclopentanecarboxylic acid methyl esterHCID 237640—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
생성물Cyclopentanecarboxylic acid, 3-hydroxy-, methyl esterHCID 520596—

반응 단계

Sodium borohydride (442.6 mg, 11.70 mmol) was added portionwise to a solution of methyl 3-oxocyclopentane-carboxylate A-10 (1.66 g, 11.70 mmol) in absolute ethanol (42.0 mL) at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for 90 mins, then quenched slowly with a 1 N aqueous solution of hydrogen chloride (10 mL), and concentrated to ca. 15 mL under reduced pressure. The aqueous layer was extracted with methylene chloride (3×50 mL); the combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated to dryness under reduced pressure to give crude methyl 3-hydroxycyclopentanecarboxylate A-11 as a yellow oil (1.33 g, Yield=79%). This material was used for next step without purification. MS (ESI), [M+1]+ 145.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637507B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-58b00e8704be473d918b838ff296efb7
출처 메모uspto-grants-2014_01