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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 27423Erstellt: 24. Oktober 2026

Water → 2-(alpha-Ethoxycarbonyl-4-chlorobenzylidene)-1-methylperhydroazepine

https://huagongshe.com/de/reaction/27423

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktEthyl (4-chlorophenyl)acetateHCID 84177—
EduktSodiumHCID 5360545—
EduktHCID 178483040HCID 178483040—
LösungsmittelEthanolHCID 702—
LösungsmittelDiethyl EtherHCID 3283—
Produkt2-(alpha-Ethoxycarbonyl-4-chlorobenzylidene)-1-methylperhydroazepineHCID 53941548—

Reaktionsschritte

Add (drop by drop at 90° in a stream of nitrogen to let the alcohol escape) a solution of 4.6 g of sodium in 100 ml of ethyl alcohol to a mixture of 53.2 g of the title compound of Example 1 and 29.8 g of ethyl 4-chlorophenylacetate. Stir it for a further 4 hours at 90° and then cool it to ambient temperature. Mix the cooled reaction mixture with 100 ml of water and 100 ml of diethyl ether, collect the organic phase and dry the latter over sodium sulfate. Concentrate the dried organic phase and then distil off any excess ethyl 4-chlorophenylacetate under a high vacuum to obtain a crude yield [15.5 g (34% of theory)] of the title compound as yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04221788
Quelldatensatzuspto-grants-1980_09
ORD IDord-ca593dee24784df38759aae09bcc0859
Quellennotizuspto-grants-1980_09