Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Benzylidene-3-quinuclidinone | HCID 243376 | — |
| Reactant | HCID 178418336 | HCID 178418336 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 10686038 | HCID 10686038 | — |
Reaction Steps
To a stirred solution of 2-benzylidene-3-oxo-1-azabicyclo[2.2.2]octane (10 g) in diethyl ether (200 ml) at -10° C. under a nitrogen atmosphere was added a solution of 2M-benzylmagnesium chloride (30 ml, in tetrahydrofuran, 50 mmol) and diethyl ether (100 ml). The solution was stirred at -10° C. for 30 minutes and at ambient temperature for 16 h. A saturated solution of aqueous ammonium chloride (200 ml) was carefully added and the product extracted into ethyl acetate. The organic phase was dried (MgSO4) and evaporated to dryness. The residue was chromatographed on a column containing silica gel 60 (220-440 mesh ASTM) eluting with mixtures of 30%, 50% and 70% ethyl acetate in petroleum ether (bp 60°-80° C.). 2-(1,2-diphenylethyl)-3-oxo1- azabicyclo [2.2.2]octane was obtained as 1:1 mixture of stereoisomers by evaporating the appropriate fractions.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05288730 |
|---|
| Source dataset | uspto-grants-1994_02 |
|---|
| ORD ID | ord-830ad8c947a84d5bb55f6c5af3b82ade |
|---|
| Source note | uspto-grants-1994_02 |
|---|