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HRID 1158883作成日:2026年10月27日

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

https://huagongshe.com/reaction/1158883

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Potassium CarbonateHCID 11430—
反応物Ammonium ChlorideHCID 25517—
反応物ThiocaprolactamHCID 3003736—
反応物Sodium MethoxideHCID 10942334—
反応物2-Bromo-3-isopropoxy-propenalHCID 53416634—
溶媒EthanolHCID 702—
溶媒DichloromethaneHCID 6344—
生成物6,7,8,9-Tetrahydro-5H-imidazo[1,2-a]azepine-2-carbaldehydeHCID 21941335—

反応条件

温度23 °C

反応手順

Thiocaprolactam (6.45 gram, 50 mmol) was dissolved in 400 ml CH2Cl2 and methyl iodide (16 ml, 5 eq) 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07812014B2
出典データセットuspto-grants-2010_10
ORD IDord-e0fb1c651ba84460aebd5b675d97b16a
出典メモuspto-grants-2010_10