HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654095Generated: October 31, 2026
8-Hydroxyquinoline → HCID 20079037, compound
https://huagongshe.com/reaction/1654095
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 8-Hydroxyquinoline | HCID 1923 | — |
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | HCID 20079037 | HCID 20079037 | — |
Reaction Steps
In 5 ml of dried THF were dissolved 200 mg of 8-hydroxyquinoline and 319 mg of the piperazine compound prepared in Example 23-(b), and 120 mg of potassium t-butoxide was further added thereto. The liquid was then stirred at room temperature for 5 days, and 20 ml of a 1N aqueous sodium hydroxide solution was poured into the liquid, followed by extracting with 100 ml of methylene chloride. Afterward, the methylene chloride solution was washed with a dilute aqueous sodium hydroxide solution, and was then dried with an anhydrous Glauber's salt. After the solvent was distilled off, the residue was purified through a silica gel column chromatograph. On allowing an effluent solvent of chloroform:methanol=50:1 to flow therethrough, the desired product 8-[3-(4-diphenylmethylpiperazine-1-yl)-2-hydroxypropoxy]-quinoline was obtained in a powdery state in an amount of 45 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05405843 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-97066ca49a0c436b8b4662ebf1996518 |
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| Source note | uspto-grants-1995_04 |
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