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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1986533Erstellt: 25. Oktober 2026

Ethyl Acetate → 4-Amino-2-methyl-1,2,4,5-tetrahydro-2-benzazepin-3-one

https://huagongshe.com/reaction/1986533

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktTrimethylsilyl iodideHCID 85247—
Eduktmethyl (2-methyl-3-oxo-2,3,4,5-tetrahydro-1H-2-benzazepin-4-yl)carbamateHCID 57722308—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-Amino-2-methyl-1,2,4,5-tetrahydro-2-benzazepin-3-oneHCID 5772230357%

Reaktionsschritte

0.6 ml of trimethylsilyl iodide is added to a solution of 203 mg (0.93 mmol) of product 2 in 10 ml of dichloromethane, and the mixture is then refluxed for 3 hours. After cooling to room temperature and adding 50 ml of ethyl acetate, the organic phase is extracted with 2×25 ml of 1N hydrochloric acid solution. The aqueous phases are combined, cooled and then basified by addition of 5N sodium hydroxide. The basic aqueous phases are then saturated with NaCl, and then extracted with 3×25 ml of ethyl acetate. The organic phases are combined, dried over magnesium sulfate and evaporated under reduced pressure to give an oily residue. This residue is chromatographed on silica gel, eluting with a 90/10 dichloromethane/methanol mixture. 100 mg (57%) of the expected product 3 are obtained in the form of an oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07550453B2
Quelldatensatzuspto-grants-2009_06
ORD IDord-36c906b80d454134ba87a400e65e03f4
Quellennotizuspto-grants-2009_06