Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2212558생성일: 2026년 10월 26일
Diethyl dimethylmalonate → 3-(4-Benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl ester
https://huagongshe.com/reaction/2212558
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl dimethylmalonate | HCID 15382 | — |
| 반응물 | 1-Bromo-4-phenylmethoxybenzene | HCID 138835 | — |
| 반응물 | CID 53628100 | HCID 178418400 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(4-Benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl ester | HCID 69596508 | 50.4% |
반응 단계
sec-Butyl lithium (5.85 mL, 7.6 mmol) was added to a solution of 1-bromo-4-benzyloxy-benzene (2.0 g, 7.6 mmol) in THF (10 mL) cooled to −78° C. under nitrogen. The reaction was stirred for 1 h and diethyl dimethylmalonate (4.29 g, 22.8 mmol) was added rapidly. This was stirred for an additional 0.5 h and then allowed to warm to room temperature. The reaction was partitioned between ethyl acetate and 1 N HCl. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated to give an oil. The product was purified by flash column chromatography (FCC) on silica gel eluting hexane:ethyl acetate (90: 10, v:v) to give 3-(4-benzyloxy-phenyl)-2,2-dimethyl-3-oxo-propionic acid ethyl ester (1.25 g, 50%) as an oil. MS found: (M+H)+=327.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07102008B2 |
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| 출처 데이터셋 | uspto-grants-2006_09 |
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| ORD ID | ord-5359d81de4724a08af69adbf01961d95 |
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| 출처 메모 | uspto-grants-2006_09 |
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