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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294820Generated: October 30, 2026

Water → 4-(Piperidin-4-yloxy)benzonitrile

https://huagongshe.com/reaction/1294820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-ChlorobenzonitrileHCID 12163—
ReactantSodium hydrideHCID 24758—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDimethylformamideHCID 6228—
Product4-(Piperidin-4-yloxy)benzonitrileHCID 11241109—

Reaction Steps

A solution of 4-hydroxy-piperidine-1-carboxylic acid tert-butyl ester (14.99 g) and 4-chlorobenzonitrile (10.35 g) in DMF (100 mL) was treated with sodium hydride (60%, 3.8 g). The resulting dark mixture was then heated to 65 C for 16 h, and allowed to cool to RT. The mixture was poured into water (1 L) and extracted with ether (3×400 mL). The combined organic phases were evaporated and the brown oil dissolved in methanol (500 mL) and treated with concentrated hydrochloric acid (20 mL). After 24 h the methanol was removed, 5% aqueous sodium hydroxide (300 mL) and water (300 mL) were added, and the mixture was extracted with DCM (3×300 mL). The combined organic phases were dried (sodium sulfate) and evaporated. Bulb to bulb distillation of the residue gave the title compound as an off white waxy solid (12.23 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241778B2
Source datasetuspto-grants-2007_07
ORD IDord-c480cce5b1354bee8575792901bce1a7
Source noteuspto-grants-2007_07