HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzyl-4-piperidone → alpha-[1-(Phenylmethyl)-4-piperidinylidene]-2-thiopheneacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | 2-Thienylacetonitrile | HCID 72880 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | alpha-[1-(Phenylmethyl)-4-piperidinylidene]-2-thiopheneacetonitrile | HCID 20278965 | — |
Reaction Steps
To a stirred mixture of 80 parts of sodium methoxide and 160 parts 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04335127 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-0fbac44957ab4e6a89251369e1f6401f |
| Source note | uspto-grants-1982_06 |