Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester | HCID 17453 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Benzyl 4-formylbicyclo[2.2.2]octane-1-carboxylate | HCID 86591749 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178499654 | HCID 178499654 | — |
Reaction Steps
Methyl (triphenylphosphoranylidene) acetate (60.2 g, 173 mmol) is added to a stirred solution of 4-formylbicyclo[2.2.2]octane-1-carboxylic acid benzyl ester (XIX, Example 94, 33.5 g, 123.2 mmol) in THF (550 ml). This mixture is then heated to gently reflux for 16 hr. The reaction mixture is cooled to 20-25° and to this is added saturated ammonium chloride (75 ml) and stirred for 10 minutes. Ethyl acetate (250 ml) and isomeric hexanes (300 ml) are added and stirred for 10 minutes. The resulting mixture is filtered through a plug of silica gel (850 g) with a thin layer of celite on the top. The solid is washed with ethyl acetate/hexane (1/1, 250 ml). The filtrates are combined and concentrated to give the title compound, NMR (400 MHz, CDCl3) δ 7.24, 6.81, 5.59, 5.01, 3.63, 1.81 and 1.48.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07579354B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-74b9777dcb7d4bd2a98574776d345f39 |
|---|
| Source note | uspto-grants-2009_08 |
|---|