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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447809Generated: October 30, 2026

2-Methylacetanilide → HCID 54072114, compound

https://huagongshe.com/reaction/1447809

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylacetanilideHCID 12107—
Reactant1-[2-(2-Chlorophenyl)ethyl]piperidin-4-oneHCID 13061538—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 54072114HCID 54072114—

Reaction Steps

48 cc of n-butyl-lithium in hexane are added dropwise at 0°, in an atmosphere of nitrogen with stirring, to a solution of 9 g of N-phenylpropionamide in 90 cc of anhydrous tetrahydrofuran. The mixture is stirred at 45°-48° for 21/2 hours and a solution of 10.5 g of N-o-chlorophenethyl-4-piperidone in 25 cc of anhydrous tetrahydrofuran is added dropwise within 50 minutes. The heating (oil bath) is removed and the reaction mixture is stirred for a further hour while cooling slowly. 10 cc of a 20% potassium carbonate solution are subsequently added to the reaction solution while stirring and cooling with ice, dilution is effected with ether and the organic phase is decanted, dried over magnesium sulphate and concentrated by evaporation at reduced pressure. The resulting crude compound is filtered over silica gel resulting crude compound is filtered over silica gel (eluant: chloroform containing 3% of methanol) and an equivalent amount of fumaric acid is added to the resulting title compound in ethanol whereby this crystallizes as hydrogen fumarate. The hydrogen fumarate form of the title compound has a M.P. of 159°-161°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04178377
Source datasetuspto-grants-1979_12
ORD IDord-9e2e011fc95346a58fb59855d7842495
Source noteuspto-grants-1979_12