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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1158883Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1158883

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktPotassium CarbonateHCID 11430—
EduktAmmonium ChlorideHCID 25517—
EduktThiocaprolactamHCID 3003736—
EduktSodium MethoxideHCID 10942334—
Edukt2-Bromo-3-isopropoxy-propenalHCID 53416634—
LösungsmittelEthanolHCID 702—
LösungsmittelDichloromethaneHCID 6344—
Produkt6,7,8,9-Tetrahydro-5H-imidazo[1,2-a]azepine-2-carbaldehydeHCID 21941335—

Reaktionsbedingungen

Temperatur23 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07812014B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-e0fb1c651ba84460aebd5b675d97b16a
Quellennotizuspto-grants-2010_10