HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 1-azabicyclo(2.2.2)octane-4-carboxylate → 1-Azabicyclo[2.2.2]oct-4-yl(di-2-thienyl)methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 1-azabicyclo(2.2.2)octane-4-carboxylate | HCID 573424 | — |
| Reactant | HCID 178418439 | HCID 178418439 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Azabicyclo[2.2.2]oct-4-yl(di-2-thienyl)methanol | HCID 68865599 | 59.5% |
Reaction Steps
A solution of 2-thienyllithium (1.0M in THF, 9.10 mL, 9.10 mmol) was chilled down to −30° C. under Ar. Ethyl 1-azabicyclo[2.2.2]octane-4-carboxylate (0.4196 g, 2.289 mmol) in THF (8 mL) was slowly added to the reaction mixture over 20 min. The reaction was allowed to warm up to room temperature over 16 h. The reaction was quenched with water and then evaporated to dryness. H2O and DCM were added, causing a light brown solid to crash out. This solid was filtered off to give the title compound (0.4161 g, 59.5%). EI-MS m/z 306(M+H+) Rt (1.35 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853404B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-38c45784d6454158b87174f507390329 |
| Source note | uspto-grants-2014_10 |