HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-{1-[Bis(2-chlorophenyl)-methyl)-piperidin-4-yl}-butyronitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Bis(2-chlorophenyl)-bromomethane | HCID 826777 | — |
| Reactant | 4-(Piperidin-4-yl)butanenitrile hydrochloride | HCID 18425704 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-{1-[Bis(2-chlorophenyl)-methyl)-piperidin-4-yl}-butyronitrile | HCID 18425745 | — |
Reaction Steps
20 g (106 mmol) 4-(3-cyanoprop-1-yl)-piperidin hydrochloride, 40.2 g (127 mmol) bis(2-chlorophenyl)-bromomethane and 35.2 g (254 mmol) potassium carbonate are heated to boiling in 90 ml acetone for six hours. After cooling, the mixture is freed from solution under vacuum. The residue is dispersed between 90 ml tolueneand 90 ml water. The aqueous phase is extracted with 10 ml tolueneand the combined organic phases are washed with 10 ml water. The organic phase is concentrated and the residue is chromatographically purified over silica gel with CHCL3. Yield: 11.2 g (27%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06451816B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-8bbe8f62ff014d25aab7bb8178ea63db |
| Source note | uspto-grants-2002_09 |