Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1405404생성일: 2026년 10월 25일
Isobutyraldehyde trimethylsilyl enol ether → Benzyl 3-methoxy-4-(2-methyl-1-oxopropan-2-yl)benzoate
https://huagongshe.com/reaction/1405404
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Isobutyraldehyde trimethylsilyl enol ether | HCID 99685 | — |
| 반응물 | Benzyl 4-bromo-3-methoxybenzoate | HCID 58551480 | — |
| 촉매 | Zinc(II) fluoride | HCID 10129912 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Benzyl 3-methoxy-4-(2-methyl-1-oxopropan-2-yl)benzoate | HCID 86668528 | — |
반응 단계
To a flask purged with nitrogen was added Pd(tBu3P)2 (26 mg, 0.050 mmol), ZnF2 (52 mg, 0.50 mmol) and DMF (4 mL). The reaction mixture was allowed to stir for 10 minutes before benzyl 4-bromo-3-methoxy-benzoate (323 mg, 1.01 mmol) was added followed by trimethyl(2-methylprop-1-enoxy)silane (277 μL, 1.51 mmol). The reaction was heated at 80° C. overnight. The crude mixture was quenched with brine and extracted with EtOAc 3 times. The organic layer was dried over sodium sulfate and the solvent was evaporated to give benzyl 3-methoxy-4-(2-methyl-1-oxopropan-2-yl)benzoate. ESI-MS m/z calc. 312.4, found 313.4 (M+1)+; Retention time: 3.27 minutes (4 min run).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08916565B2 |
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| 출처 데이터셋 | uspto-grants-2014_12 |
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| ORD ID | ord-a69e54d1aad34fee997f6f535585fb9b |
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| 출처 메모 | uspto-grants-2014_12 |
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