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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Tert.butyl-1-chloro-4-phenyl isoquinoline | HCID 20385843 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Tert.butyl-4-phenyl isoquinoline hydrochloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04175191 |
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| Source dataset | uspto-grants-1979_11 |
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| ORD ID | ord-f75499ac04ce451bbe59d2d5cc63ef1c |
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| Source note | uspto-grants-1979_11 |
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