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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2216587생성일: 2026년 10월 25일

Methyl iodide → 6,7,8,9-Tetrahydro-5H-imidazo[1,2-a]azepine-2-carbaldehyde

https://huagongshe.com/reaction/2216587

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Potassium CarbonateHCID 11430—
반응물Ammonium ChlorideHCID 25517—
반응물ThiocaprolactamHCID 3003736—
반응물Sodium MethoxideHCID 10942334—
반응물2-Bromo-3-isopropoxy-propenalHCID 53416634—
용매EthanolHCID 702—
용매DichloromethaneHCID 6344—
생성물6,7,8,9-Tetrahydro-5H-imidazo[1,2-a]azepine-2-carbaldehydeHCID 21941335—

반응 조건

온도23 °C

반응 단계

Thiocaprolactam (6.45 gram, 50 mmol) was dissolved in 400 ml CH2Cl2 and methyl iodide (16 ml, 5eq) was next added. The mixture was stirred under nitrogen for 18 hrs. Then it was treated with 100 ml potassium carbonate (50%, aq.). The organic layer was then dried over magnesium sulfate. After filtration and concentration 7.3 gram of material was obtained. This material was dissolved 300 ml ethanol and 2.83 gram of ammonium chloride was added. The mixture was refluxed for 1 hr. Then the solvent was removed in vacuo. Half of the material was added 200 ml ethanol and then followed by addition of 1.35 gram (25 mmol) sodium methoxide and 4.8 gram (25 mmol) 2-Bromo-3-isopropoxy-propenal and the mixture was stirred at 23° C. for 2 hrs. Then the solvent was removed and 200 ml chloroform was added along with 10 ml triethyl amine. The mixture was refluxed for 2 hrs and then cooled to 23° C. The reaction media was partitioned between 300 ml DCM and 2×150 potassium carbonate (50%). The organic layer was dried over magnesium sulfate. After filtration and concentration 2.1 gram of oil product was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07112582B2
출처 데이터셋uspto-grants-2006_09
ORD IDord-30a8ea4dce4941f8b096b74c36d35b25
출처 메모uspto-grants-2006_09