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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866054Generated: November 2, 2026

Water → 4-cyano-N-(4-propoxyphenylmethyl)piperidine

https://huagongshe.com/reaction/866054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ChlorideHCID 5234—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant4-aminocarbonyl-N-(4-propoxyphenylmethyl)piperidineHCID 19040932—
Solvent1,2-DichloroethaneHCID 11—
Product4-cyano-N-(4-propoxyphenylmethyl)piperidineHCID 1904091356.1%

Reaction Steps

A mixture of 27.0 grams (0.10 mole) of 4-aminocarbonyl-N-(4-propoxyphenylmethyl)piperidine in 200 mL of 1,2-dichloroethane was stirred at ambient temperature, and 8.0 grams (0.14 mole) of sodium chloride, followed by 9.2 grams (0.06 mole) of phosphorous oxychloride were added. The reaction mixture was then warmed to reflux, where it stirred for about 1.75 hours. The reaction mixture was cooled to ambient temperature and about 350 mL of water was added. The aqueous layer was separated, washed with two portions of diethyl ether, and then made basic with aqueous 5% sodium hydroxide. The mixture was extracted with two portions of diethyl ether. The combined extracts were washed with an aqueous solution saturated with sodium chloride. The organic layer was dried with sodium sulfate and poured through a pad of silica gel. The silica gel pad was washed with 1000 mL of diethyl ether. The combined eluants were concentrated under reduced pressure, yielding 14.5 grams of 4-cyano-N-(4-propoxyphenylmethyl)piperidine. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05569664
Source datasetuspto-grants-1996_10
ORD IDord-f90e01630c18444380480542283994c6
Source noteuspto-grants-1996_10