HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644119Generated: October 30, 2026
Chloroform → 4-[3-(4-Piperidinyl)propoxy]benzonitrile
https://huagongshe.com/reaction/644119
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 86625834 | HCID 86625834 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[3-(4-Piperidinyl)propoxy]benzonitrile | HCID 59263019 | — |
Reaction Steps
To a chloroform (100 mL) solution of 14.0 g of tert-butyl=4-[3-(4-cyanophenoxy)propyl]-1-piperidinecarboxylate was dropwise added 40 mL of trifluoroacetic acid under cooling with water over a period of 10 minutes. This mixture was stirred at the same temperature for 20 minutes, and then stirred at room temperature for 35 minutes. After distilling off the solvent under reduced pressure, chloroform and water were added. A sodium hydroxide aqueous solution was added thereto for adjustment to pH 13.0. The organic layer was separated, and the aqueous layer was extracted with chloroform. The organic layer and the extract were combined, which was then washed with a sodium hydroxide aqueous solution and dried with potassium carbonate, followed by distilling off the solvent under reduced pressure to provide 10.3 g of 4-[3-(4-piperidinyl)propoxy]benzonitrile as pale yellow solid form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700623B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-88f6f8316ef541f39b271d649f9975e7 |
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| Source note | uspto-grants-2010_04 |
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