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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130905생성일: 2026년 10월 26일

Hydrogen Peroxide → Ammonium Bicarbonate

https://huagongshe.com/reaction/130905

반응식

참여 물질

역할이름HCID투입량
반응물Hydrogen PeroxideHCID 784—
반응물IsoamylamineHCID 7894—
반응물EthylvanillinHCID 8467—
반응물Potassium CarbonateHCID 11430—
반응물4-FluorobenzonitrileHCID 14517—
용매DimethylformamideHCID 6228—
생성물Ammonium BicarbonateHCID 14013—
생성물HCID 59729983HCID 59729983—

반응 조건

온도130 °C

반응 단계

Dissolve 3-ethoxy-4-hydroxy-benzaldehyde (2.57 g, 15.45 mmol) in DMF (20 mL), add K2CO3 (2.33 g, 16.86 mmol) and 4-fluorobenzonitrile (1.70 g, 14.05 mmol), heat the mixture at 130° C. overnight. Add water and extract the aqueous layer with EtOAc. Combine organic layers and dry over Na2SO4. Eliminate the solvent and purify by flash chromatography on silica gel (eluent: EtOAc/hexane 15/85) to get a mixture of two compounds (1.45 g). This mixture (240 mg) is submitted to the reductive amination conditions described for compound 1 (step 3) using 3-methyl-butylamine to obtain a mixture of two compounds which is subject to hydrolysis using hydrogen peroxide and potassium carbonate in the conditions described elsewhere in this document. This mixture is purified by flash chromatography (EtOAc and CH2Cl2/MeOH 10%) and then the title compound is isolated after HPLC (Column: XTerraMSC18 (5 um, 19×100 mm). Isocratic mode: 55/45 Ammonium bicarbonate-pH 9-/Acetonitrile. Flow: 10 mL/min).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381719B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-cc0e8454054e4ccdb4c60b683943b774
출처 메모uspto-grants-2008_06