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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405930Generated: October 30, 2026

Diethyl Ether → HCID 58117883, compound

https://huagongshe.com/reaction/405930

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
Reactant1-Benzyl-4-(4-fluoro-phenyl)-piperidine-4-carbonitrileHCID 54497189—
SolventTolueneHCID 1140—
ProductHCID 58117883HCID 58117883—

Reaction Steps

Under argon 11.86 g magnesium chips are placed in 50 ml anhydrous diethyl ether, then a solution of 85.4 g 4-bromofluorobenzene in 200 ml anhydrous diethyl ether is slowly added dropwise. The reaction mixture is stirred for 2 h at reflux temperature and then cooled to ambient temperature. A solution of 45.4 g 1-benzyl-4-(4-fluoro-phenyl)-piperidine-4-carbonitrile in 100 ml anhydrous toluene is added dropwise. The diethyl ether is distilled off and the remainder of the reaction mixture is stirred overnight at 80° C. After cooling the reaction mixture is combined with 500 ml ice water and 100 g NH4Cl and the product is extracted with ethyl acetate. The organic phase is washed with water and sat. NaCl solution, dried and evaporated to dryness. 70 ml glacial acetic acid and 20 ml sulphuric acid 33% are added to the residue. The reaction mixture is heated to 100° C., then cooled, combined with ice water and adjusted to pH ˜9 with 4N NaOH. Then 250 ml diisopropylether are added. The reaction mixture is then stirred overnight at ambient temperature. The precipitate formed is suction filtered, washed with diisopropylether and water and dried. 42.7 g product are obtained as a solid. M.p: 136-138.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754073B2
Source datasetuspto-grants-2014_06
ORD IDord-eff06ed1936f4b1b87353cc17dd7f1aa
Source noteuspto-grants-2014_06