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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1701876Erstellt: 25. Oktober 2026

1,2,3,4-Tetrahydroisoquinoline → 1-(2-Chlorophenoxy)-4-(1,2,3,4-tetrahydroisoquinolyl)-2-butanol Hydrochloride Hydrate

https://huagongshe.com/reaction/1701876

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2,3,4-TetrahydroisoquinolineHCID 7046—
Edukt1-(o-Chlorophenoxy)-2-hydroxybutyl chlorideHCID 19840239—
EduktHydrate;hydrochlorideHCID 21885828—
Lösungsmittel1-ButanolHCID 263—
Produkt1-(2-Chlorophenoxy)-4-(1,2,3,4-tetrahydroisoquinolyl)-2-butanol Hydrochloride HydrateHCID 21274581—

Reaktionsschritte

A mixture of 11.8 g. (0.05 mole) of 1-(2-chlorophenoxy)-2-hydroxybutyl chloride, 13.3 g. (0.1 mole) of 1,2,3,4-tetrahydroisoquinoline and 100 ml. of n-butanol was heated in a steel bomb at 120° C. for 24 hr. The reaction mixture was filtered at room temperature, the filtrate was mixed with 200 ml. 3 N hydrochloric acid and extracted twice with 100 ml. isopropyl ether. The aqueous acidic solution was made basic and extracted with isopropyl ether and treated with ethereal hydrogen chloride. Recrystallization with isopropanol yielded 6 g. of the hydrochloride hydrate of the product which melted at 118°-120° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04379167
Quelldatensatzuspto-grants-1983_04
ORD IDord-e5d85056756c437f9baab21848fab3a5
Quellennotizuspto-grants-1983_04