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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437561Generated: October 30, 2026

Benzene, 1-chloro-4-fluoro- → 1-Benzyl-4-(p-chlorophenoxy)piperidine

https://huagongshe.com/reaction/437561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzene, 1-chloro-4-fluoro-HCID 9604—
ReactantSodium hydrideHCID 24758—
Reactant1-Benzylpiperidin-4-olHCID 78461—
ReactantHCID 178418361HCID 178418361—
SolventDimethylformamideHCID 6228—
Product1-Benzyl-4-(p-chlorophenoxy)piperidineHCID 21428714—

Reaction Steps

A solution of 21.6 g of 1-benzyl-4-piperidinol in 75ml. of dimethylformamide is added slowly to a stirred suspension of 8.7 g of a 50% oil dispersion of sodium hydride in 225 ml. of dimethylformamide at 60°-70° C. After addition is complete stirring and heating are continued until no more hydrogen gas is liberated. A solution of 19.6 g of 1-chloro-4-fluorobenzene in 75 ml. of dimethylformamide is added, and the solution is permitted to stir at 65°-70° C. for 16 hours. After cooling to ambient temperature, the solution is poured into 600 ml. of water, the aqueous solution is extracted with benzene, the benzene extracts are dried, and the benzene is removed under reduced pressure, leaving a yellow oil of 1-benzyl-4-(p-chlorophenoxy)piperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031221
Source datasetuspto-grants-1977_06
ORD IDord-fcf69e8b36014cb8b24ac1ad22295f2d
Source noteuspto-grants-1977_06