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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 127484Erstellt: 24. Oktober 2026

Ethanolamine → 2,2-Dichloro-1-(8-methyl-1-oxa-4-azaspiro[4.5]decan-4-yl)ethan-1-one

https://huagongshe.com/de/reaction/127484

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
EduktPyridineHCID 1049—
EduktDichloroacetyl chlorideHCID 6593—
Edukt4-MethylcyclohexanoneHCID 11525—
Produkt2,2-Dichloro-1-(8-methyl-1-oxa-4-azaspiro[4.5]decan-4-yl)ethan-1-oneHCID 13277204—

Reaktionsschritte

From a boiling mixture of 11.2 g. (0.1 moles) of 4-methyl-cyclohexanone and 6.1 g. (0.1 moles) of ethanolamine in 100 ml. of benzene the formed water is continuously distilled off. Boiling is continued until 1.8 ml. of water are separated. The reaction mixture is then cooled and 8 g. (0.1 moles) of pyridine are added followed by dropwise addition of 14.7 g. (0.1 moles) of dichloroacetyl chloride with external salt/ice cooling. Further following the procedure described in Example 2, 20.7 g. (0.078 moles) of a rose, oily product are obtained. Recrystallization from absolute ethanol affords a white, crystalline product melting at 119° to 120° C. The structure of the compound obtained can be verified by IR spectrum analysis.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04256481
Quelldatensatzuspto-grants-1981_03
ORD IDord-7e8eee49de1241f0a4981066e19cc3e7
Quellennotizuspto-grants-1981_03