HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(3-Piperidinomethylphenylthio)butyronitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Reactant | 3-(Piperidin-1-ylmethyl)benzenethiol | HCID 13505507 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(3-Piperidinomethylphenylthio)butyronitrile | HCID 21294554 | — |
Reaction Steps
A stirred suspension of 3-piperidinomethylthiophenol (0.36 g) in dry dimethylformamide (4 ml) was treated with anhydrous potassium carbonate (0.5 g) and stirred for 30 minutes. 4-Bromobutyronitrile (0.18 ml) was then added to the reaction mixture with dimethylformamide (1 ml) and the resultant suspension stirred at room temperature for 48 hours. The resulting product was poured into 5 volumes of water and extracted with ethyl acetate; the extracts were washed with water, dried and evaporated to give 4-(3-piperidinomethylphenylthio)butyronitrile as an orange-red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04767769 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-f943add7633e41be847802063bf84698 |
| Source note | uspto-grants-1988_08 |