HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447809Generated: October 30, 2026
2-Methylacetanilide → HCID 54072114, compound
https://huagongshe.com/reaction/1447809
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methylacetanilide | HCID 12107 | — |
| Reactant | 1-[2-(2-Chlorophenyl)ethyl]piperidin-4-one | HCID 13061538 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 54072114 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04178377 |
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| Source dataset | uspto-grants-1979_12 |
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| ORD ID | ord-9e2e011fc95346a58fb59855d7842495 |
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| Source note | uspto-grants-1979_12 |
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