HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790429Generated: October 26, 2026
Acetic Acid → 1-(1-Acetylpiperidin-4-yl)indoline
https://huagongshe.com/reaction/1790429
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Indoline | HCID 10328 | — |
| Reactant | N-Acetyl-4-piperidone | HCID 122563 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(1-Acetylpiperidin-4-yl)indoline | HCID 22038075 | 82.2% |
Reaction Steps
Indoline (25 ml), 1-acetyl-4-piperidone (25 g) and glacial acetic acid (20 ml) were dissolved in methanol (300 ml). After adding 10% palladium carbon (1.0 g) thereto, catalytic reduction was carried out under atmospheric pressure. After the completion of the reaction, the reaction solution was filtered through celite, washed with methanol and concentrated under reduced pressure. The residue was partitioned between water and ethyl acetate and basified with a 5 N aqueous solution of sodium hydroxide followed by extraction with ethyl acetate. The ethyl acetate layer was washed with water and brine, dried and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane system) to give the title compound (35.6 g) as a pale yellow wax (yield: 82.2%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071201B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-ccb9223705f34e2f950d70ce02420337 |
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| Source note | uspto-grants-2006_07 |
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