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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64699Generated: October 26, 2026

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

https://huagongshe.com/reaction/64699

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,3,4-TetrahydroisoquinolineHCID 7046—
Reactant1-(o-Chlorophenoxy)-2-hydroxybutyl chlorideHCID 19840239—
ReactantHydrate;hydrochlorideHCID 21885828—
Solvent1-ButanolHCID 263—
Product1-(2-Chlorophenoxy)-4-(1,2,3,4-tetrahydroisoquinolyl)-2-butanol Hydrochloride HydrateHCID 21274581—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609735
Source datasetuspto-grants-1986_09
ORD IDord-2cd7907767c94e6caa7389cf9b916e6c
Source noteuspto-grants-1986_09