HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 19007316, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,2-Diphenyl-2-(pyrrolidin-3-yl)acetamide | HCID 13633754 | — |
| Reactant | 4-(2-Bromoethyl)-1,2-dimethylbenzene | HCID 22507320 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19007316 | HCID 19007316 | — |
Reaction Steps
A mixture containing 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)pyrrolidine (0.5 g--see Preparation 8), 3,4-dimethylphenethyl bromide (0.4 g--see Preparation 18), anhydrous potassium carbonate (0.5 g) and acetonitrile (10 ml) was heated under reflux for 2 hours. On cooling to room temperature, water (80 ml) was added and the mixture was extracted with dichloromethane (3×70 ml). The combined dichloromethane extracts were dried (MgSO4) and concentrated in vacuo to give a yellow oil which was purified by column chromatography on silica eluting with dichloromethane containing methanol (0% up to 4%). The product-containing fractions were combined and concentrated in vacuo to give the title compound as an oil, yield, 0.22 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05340831 |
| Source dataset | uspto-grants-1994_08 |
| ORD ID | ord-c079336a170d43f9a11eef2160f1e429 |
| Source note | uspto-grants-1994_08 |