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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

반응식

참여 물질

역할이름HCID투입량
반응물Isobutyraldehyde trimethylsilyl enol etherHCID 99685—
반응물Benzyl 4-bromo-3-methoxybenzoateHCID 58551480—
촉매Zinc(II) fluorideHCID 10129912—
용매DimethylformamideHCID 6228—
생성물Benzyl 3-methoxy-4-(2-methyl-1-oxopropan-2-yl)benzoateHCID 86668528—

반응 조건

온도80 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08916565B2
출처 데이터셋uspto-grants-2014_12
ORD IDord-a69e54d1aad34fee997f6f535585fb9b
출처 메모uspto-grants-2014_12