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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 881026Generated: November 1, 2026

Chloroform → 4-[3-(4-Piperidinyl)propoxy]benzonitrile

https://huagongshe.com/reaction/881026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59263075HCID 59263075—
SolventWaterHCID 962—
Product4-[3-(4-Piperidinyl)propoxy]benzonitrileHCID 59263019103.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993603B2
Source datasetuspto-grants-2015_03
ORD IDord-8d577147c50745679ae781d7c3d79011
Source noteuspto-grants-2015_03