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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 657555Erstellt: 25. Oktober 2026

Triethylamine → 3-Acryloyl-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepine

https://huagongshe.com/reaction/657555

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktAcryloyl chlorideHCID 13140—
Edukt7,8-dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochlorideHCID 22004098—
LösungsmittelDichloromethaneHCID 6344—
Produkt3-Acryloyl-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepineHCID 68532781—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

At ambient temperature, 70 g (287.2 mmol) of the product obtained in Step 2 are dissolved in 1200 mL of dichloromethane, and then 100 mL (718 mmol/2.5 eq.) of triethylamine are added all at once. The mixture is brought to 0° C. and a solution of 25.8 mL (315.9 mmol/1.1 eq.) of acryloyl chloride in 270 mL of dichloromethane is poured in dropwise, maintaining the temperature at about 0° C. After 2 hours at 0° C., the mixture is stirred at ambient temperature overnight. Washing with 750 mL of water, 750 mL of 1N hydrochloric acid and 750 mL of water and then drying over magnesium sulphate are then carried out. After filtration and evaporation, the residue is chromatographed over 3.2 kg of silica (eluant: dichloromethane/ethanol: 95/5), followed by recrystallisation from isopropanol. After filtration over a frit and drying in vacuo at 50° C., the desired product is obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08076325B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-01fa4a3c5f0240519da7d7926605189f
Quellennotizuspto-grants-2011_12