HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20356907, compound → HCID 20356904, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20356907 | HCID 20356907 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Product | HCID 20356904 | HCID 20356904 | — |
Reaction Steps
1 Part of 3,3-(diphenyl)-3-(2-thienyl)propionyl chloride (Martenson and Nilson Acta Chem. Scand. 19 711, (1965) is reacted with 20 parts of 2-azabicyclo[2.2.2]octane in 50 parts of benzene. The precipitated amide is filtered and the benzene solution washed with water, dried with magnesium sulfate, and the benzene evaporated. The remaining oil is crystallized to provide 2-[3,3-diphenyl-3-(2-thienyl)propionyl]2-azabicyclo[2.2.2]octane. This amide is reduced with lithium aluminum hydride as described in Example 1 to provide 2-[3,3-diphenyl-3-(2-thienyl)propyl]2-azabicyclo[2.2.2]octane. This compound has the following structural formula ##STR34##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04086227 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-a0cc4b7b17ea43538683d4b0024f16af |
| Source note | uspto-grants-1978_04 |