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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1360783생성일: 2026년 10월 27일

Methanol → [(E)-3-(4-formyl-3,5-dimethylphenyl)-allyl]-phosphonic acid diethyl ester

https://huagongshe.com/reaction/1360783

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Diethyl allylphosphonateHCID 573014—
반응물Sodium NitriteHCID 23668193—
반응물3-(4-{6-[5-(4-Methoxy-phenylamino)-[1,3,4]oxadiazol-2-yl]-1H-benzoimidazol-2-yl}-3,5-dimethyl-phenyl)-propionic acid methyl esterHCID 66966816—
촉매palladium(II) acetateHCID 167845—
용매WaterHCID 962—
용매Tetrafluoroboric acidHCID 28118—
생성물[(E)-3-(4-formyl-3,5-dimethylphenyl)-allyl]-phosphonic acid diethyl esterHCID 86632823—

반응 조건

온도0 °C

반응 단계

To a suspension of 4-amino-2,6-dimethylbenzaldehyde (3.0 g, 20.1 mmol) (Example 1-60, step B) in enough 42% HBF4 to be stirred at 0° C. was added a solution of NaNO2 (1.39 g, 20.1 mmol) in water (10 ml) slowly. After 30 min at 0° C., MeOH (50 mL) was added and followed by Pd(OAc)2 (677 mg) and diethyl allylphosphonate (5.38 g, 30.2 mmol). The reaction mixture was heated at 80° C. for 30 min and the suspension was filtered through Celite, washed with CH2Cl2. The filtrate was extracted with CH2Cl2 and the combined organic layers were washed with water, brine, dried with MgSO4, and filtered. The solvent was removed under reduced pressure and the residue was purified by flash chromatography using a gradient of heptane/EtOAc (10:1 to 5:1 then followed by 100% EtOAc) to give the title compound as a light yellow oil. MS: m/z 311 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07879850B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-66bd870ee3284d83b6b1ff5d37893e27
출처 메모uspto-grants-2011_02