Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Bromo-2,2-diphenylbutyronitrile | HCID 96575 | — |
| Reactant | 2-Azabicyclo[2.2.2]octane hydrochloride | HCID 21984844 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | HCID 20356962 | HCID 20356962 | 76.8% |
Reaction Steps
To a stirred solution of 0.85 part of 2-azabicyclo-[2.2.2.]octane hydrochloride in 20 parts of water is added 0.71 part of potassium hydroxide under a nitrogen atmosphere. Then, 1.90 parts of 2,2-diphenyl-4-bromobutyronitrile is added, and the mixture heated to reflux for 3.5 hours. This reaction mixture is cooled to about 60° C., whereupon 13 parts of benzene is added. The aqueous layer is separated and extracted with 15 parts of benzene. To the combined benzene extracts is added dropwise 2 parts by volume of a solution of hydrochloric acid in isopropanol. The volume of this solution is reduced by heating on a steam bath. Cooling affords a white precipitate which is washed with benzene and dried at 100° C. for about 2 hours. The resulting product, 2,2-diphenyl-4-(2-azabicyclo[2.2.2]oct-2-yl)butyronitrile hydrochloride, is obtained in approximately 76.8% yield. This product melts at about 194° - 197° C., and is represented by the following structural formula. ##STR11##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04086234 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-ea72855d2b16432097a1b573c9cb1204 |
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| Source note | uspto-grants-1978_04 |
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