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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 726696Erstellt: 24. Oktober 2026

Dimethyl Sulfate → 5-methoxy-1-tosyl-2,3-dihydro-1H-1-benzazepine

https://huagongshe.com/de/reaction/726696

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethyl SulfateHCID 6497—
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
Edukt1-Tosyl-3,4-dihydro-1H-benzo[b]azepin-5(2H)-oneHCID 266852—
LösungsmittelDimethylformamideHCID 6228—
Produkt5-methoxy-1-tosyl-2,3-dihydro-1H-1-benzazepineHCID 11381909—

Reaktionsschritte

In 10 ml of dimethylformamide was suspended 165 mg of 60% sodium hydride, and 1.0 g of 1-tosyl-2,3,4,5-tetrahydro-1-H-1 -benzazepin-5-one was added to the suspension under ice-cooling, followed by 1 hour of stirring in the ice bath. To this was added dropwise 0.90 ml of dimethyl sulfate, and the mixture was stirred for 30 minutes. After adding ammonium chloride aqueous solution to the reaction solution and subsequently evaporating the solvent, the thus obtained residue was treated with chloroform and water to effect phase separation, and the resulting organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated and the resulting residue was applied to column chromatography, which was eluted with hexane-ethyl acetate (4:1, v/v) to obtain 621 mg of 5-methoxy-1-tosyl-2,3-dihydro-1H-1-benzazepine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05710150
Quelldatensatzuspto-grants-1998_01
ORD IDord-19a228057e4c429da16d281f45916afa
Quellennotizuspto-grants-1998_01