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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46814Generated: October 30, 2026

Potassium Hydroxide → 3-Tert.butyl-4-phenyl isoquinoline hydrochloride

https://huagongshe.com/reaction/46814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant3-Tert.butyl-1-chloro-4-phenyl isoquinolineHCID 20385843—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-Tert.butyl-4-phenyl isoquinoline hydrochlorideHCID 20385855—

Reaction Steps

A mixture of 21.7 g. (0.073 mole) of 3-tert.butyl-1-chloro-4-phenyl isoquinoline, 4.09 g. (0.073 mole) potassium hydroxide, 1.09 g 10% palladium on carbon and 1 liter of ethanol is hydrogenated at room temperature and 50 psi until 1 equivalent of hydrogen is absorbed. The catalyst is filtered off and washed with ethanol, combined ethanol portions are evaporated in vacuo. The residue is dissolved in ethyl ether, washed with water, dried, and filtered and the filtrate treated with gaseous HCl. The resulting white solid is filtered and recrystallized from ethanolethyl ether, washed with water, dried, and filtered and the filtrate treated with gaseous HCl. The resulting white solid is filtered and recrystallized from ethanol-ethyl ether (1:1) to give 3-tert.butyl-4-phenyl isoquinoline hydrochloride; m.p. 236°-238° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04175191
Source datasetuspto-grants-1979_11
ORD IDord-f75499ac04ce451bbe59d2d5cc63ef1c
Source noteuspto-grants-1979_11