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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463131Generated: October 25, 2026

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

https://huagongshe.com/reaction/1463131

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 numberUS04463190
Source datasetuspto-grants-1984_07
ORD IDord-fd54694a01cf4b7e89baf09bc9b8d539
Source noteuspto-grants-1984_07