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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1453318생성일: 2026년 10월 26일

Methyl acetoacetate → 5-Cyclopentyl-5-hydroxy-9-(4-hydroxy-2,5-dimethyl-phenyl)-3-oxo-non-8-ynoic Acid Methyl Ester

https://huagongshe.com/reaction/1453318

반응식

참여 물질

역할이름HCID투입량
반응물Methyl acetoacetateHCID 7757—
반응물Lithium diisopropylamideHCID 2724682—
반응물1-Cyclopentyl-5-(4-hydroxy-2,5-dimethyl-phenyl)-pent-4-yn-1-oneHCID 58762502—
용매TetrahydrofuranHCID 8028—
생성물5-Cyclopentyl-5-hydroxy-9-(4-hydroxy-2,5-dimethyl-phenyl)-3-oxo-non-8-ynoic Acid Methyl EsterHCID 5876239748.3%

반응 단계

To a freshly prepared solution of LDA (1 M, 2.2 mL, 2.2 mmol) cooled to 0° C. was added methyl acetoacetate (0.12 mL, 1.1 mmol) dissolved in THF (1 mL). After stirring for 30 minutes, 1-cyclopentyl-5-(4-hydroxy-2,5-dimethyl-phenyl)-pent-4-yn-1-one (0.10 g, 0.37 mmol) from Step 1 above dissolved in THF (1 mL) was added. The reaction was stirred for 1Hour, and then warmed to room temperature. After quenching with 10 mL saturated ammonium chloride, the layers were separated. The aqueous layer was extracted with 2×15 mL CH2Cl2, and the organic layers were combined. After drying over Na2SO4, and filtering to remove the solids, the mother liquor was concentrated to an oil. Flash chromatography of the oil gave the desired product (69 mg, 48% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07473790B2
출처 데이터셋uspto-grants-2009_01
ORD IDord-def68bf565c74f419f2ccceeab3b2ce1
출처 메모uspto-grants-2009_01