HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597227Generated: October 31, 2026
HCID 22759845, compound → HCID 22759851, compound
https://huagongshe.com/reaction/597227
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22759845 | HCID 22759845 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22759851 | HCID 22759851 | — |
Reaction Steps
18.9 Parts of a mixture of the two isomers (cis and trans) of 2-(2,2-diphenylethylidenyl)-1-azabicyclo[2.2.2]-octan -3-one, and 2-(2,2-diphenylethenyl)-1-azabicyclo[2.2.2]-octan-3-one is dissolved in approximately 790 parts ethanol. Then, 4 parts of a 5% palladium-on-carbon catalyst is added and the mixture shaken in a Parr Shaker at room temperature and a pressure of 36-60 psi for 3 hours. The catalyst is removed by filtration and the solvents removed in vacuo. The residual white solid is dissolved in 560 parts of hot n-pentane. The solution is filtered and then concentrated on a steam bath to a volume of about 190 ml. Standing at room temperature affords a precipitate which is filtered, washed with n-pentane and dried in vacuo to provide a white solid. This solid is recrystallized from ethyl ether to afford 2-(2,2-diphenylethyl)-1-azabicyclo[2.2.2]octan-3-one. This compound begins to shrink at 103° C., clouds at 104°-105° C. and melts at about 107° C. and is represented by the following structural formula. ##STR9##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04013667 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-7a1f44cafbd344eca557cbd23fc4b562 |
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| Source note | uspto-grants-1977_03 |
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