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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 414825Erstellt: 24. Oktober 2026

Water → HCID 14349113, Verbindung

https://huagongshe.com/de/reaction/414825

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktDimethylformamideHCID 6228—
EduktSodium hydrideHCID 24758—
Edukt1,2-Dichloro-4-fluorobenzeneHCID 74028—
EduktHCID 13118512HCID 13118512—
ProduktHCID 14349113HCID 1434911357%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

A solution of 7,8-dimethoxy-1-hydroxy-2,3,4,5-tetrahydro-3-benzazepine (3 g, 13.4 mmole) in 25 ml dimethylformamide was slowly dropped into a stirring suspension of sodium hydride (50% oil dispersion, 0.7 g, 14.8 mmole), previously washed with hexane, in 10 ml dimethylformamide. After the addition was completed, the mixture was warmed for one hour at 60° C., then was cooled and a solution of 3,4-dichlorofluorobenzene (2.4 g, 14.8 mmole) in 10 ml dimethylformamide was added. After stirring two hours at ambient temperature, the reaction mixture was stirred with 400 ml water and was extracted with ethyl acetate. The organic extract was washed with ethyl acetate. The organic extract was washed with water and saturated NaCl and was dried (anhydrous MgSO4), filtered and evaporated to 7 g of an oil. This oil was purified by HPLC (silica gel, 5% methanol in dichloromethane) to give 2.8 g (57%) of an oil. This oil was converted to the oxalate salt as in Example 1 and was recrystallized from ethyl acetate-methanol to give 2.1 g (34%) of 1,(3-4-dichlorophenoxy)-7,8-dimethoxy-2,3,4,5-tetrahydro-3-benzazepine oxalate, d 167°-168° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04794181
Quelldatensatzuspto-grants-1988_12
ORD IDord-ec49c880435b4f18b7729301aa2b6e48
Quellennotizuspto-grants-1988_12