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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248233Generated: October 26, 2026

1-Benzyl-4-piperidone → alpha-[1-(Phenylmethyl)-4-piperidinylidene]-2-thiopheneacetonitrile

https://huagongshe.com/reaction/1248233

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-piperidoneHCID 19220—
Reactant2-ThienylacetonitrileHCID 72880—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Productalpha-[1-(Phenylmethyl)-4-piperidinylidene]-2-thiopheneacetonitrileHCID 20278965—

Reaction Steps

To a stirred mixture of 80 parts of sodium methoxide and 160 part of methanol are added successively 50 parts of 2-thiopheneacetonitrile and then dropwise 66 parts of 1-(phenylmethyl)-4-piperidinone. Upon completion, the whole is heated to reflux and stirring at reflux temperature is continued for one hour. The reaction mixture is cooled and evaporated. The residue is distilled in a molecular distillation-apparatus, yielding about 70 parts of α-[1-(phenylmethyl)-4-piperidinylidene]-2-thiopheneacetonitrile as a residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04522945
Source datasetuspto-grants-1985_06
ORD IDord-921f3de8f7954855a384c12325968c35
Source noteuspto-grants-1985_06