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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Acryloyl chloride | HCID 13140 | — |
| Edukt | 7,8-dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride | HCID 22004098 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-Acryloyl-7,8-dimethoxy-2,3,4,5-tetrahydro-1H-3-benzazepine | HCID 68532781 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08076325B2 |
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| Quelldatensatz | uspto-grants-2011_12 |
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| ORD ID | ord-01fa4a3c5f0240519da7d7926605189f |
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| Quellennotiz | uspto-grants-2011_12 |
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