HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378518Generated: November 3, 2026
1-Benzyl-4-(1-indolyl)-piperidine → 1-(Piperidin-4-yl)-1H-indole
https://huagongshe.com/reaction/1378518
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Benzyl-4-(1-indolyl)-piperidine | HCID 21222225 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(Piperidin-4-yl)-1H-indole | HCID 14090755 | 80% |
Reaction Steps
A glacial acetic acid (15 mL) solution containing Pd(OH)2 /C and 1-benzyl-4-(1-indolyl)-piperidine was placed under an H2 atmosphere. The reaction temperature was raised to 80° C. After 1 hour, the reaction was cooled to room temperature and filtered. The filtrate was made basic (pH 8-9) with saturated NaHCO3, and extracted with methylene chloride. The extract was washed with water, dried, and concentrated. This material was sufficiently pure for further reactions giving 1.09 g (80% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05668152 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-fd5208d206c84840b4cc241fac2c21b0 |
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| Source note | uspto-grants-1997_09 |
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