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HRID 1382393作成日:2026年10月26日

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

https://huagongshe.com/reaction/1382393

反応式

関与物質

役割名称HCID仕込み量
反応物1,2,3,4-TetrahydroisoquinolineHCID 7046—
反応物1-(o-Chlorophenoxy)-2-hydroxybutyl chlorideHCID 19840239—
反応物Hydrate;hydrochlorideHCID 21885828—
溶媒1-ButanolHCID 263—
生成物1-(2-Chlorophenoxy)-4-(1,2,3,4-tetrahydroisoquinolyl)-2-butanol Hydrochloride HydrateHCID 21274581—

反応手順

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. 3N 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04806555
出典データセットuspto-grants-1989_02
ORD IDord-9bfb7643045647b98f7ad1e1d668f317
出典メモuspto-grants-1989_02