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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methyl acetoacetate | HCID 7757 | — |
| 반응물 | Lithium diisopropylamide | HCID 2724682 | — |
| 반응물 | 1-Cyclopentyl-5-(4-hydroxy-2,5-dimethyl-phenyl)-pent-4-yn-1-one | HCID 58762502 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 5-Cyclopentyl-5-hydroxy-9-(4-hydroxy-2,5-dimethyl-phenyl)-3-oxo-non-8-ynoic Acid Methyl Ester | HCID 58762397 | 48.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07473790B2 |
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| 출처 데이터셋 | uspto-grants-2009_01 |
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| ORD ID | ord-def68bf565c74f419f2ccceeab3b2ce1 |
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| 출처 메모 | uspto-grants-2009_01 |
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