Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl 2-oxo-1-pyrrolidineacetate | HCID 108835 | — |
| Reactant | (Hexahydro-1H-pyrrolizin-7A-YL)methanamine | HCID 10654304 | — |
| Product | HCID 177933 | HCID 177933 | — |
Reaction Steps
A mixture consisting of 14.1 g (89.6 mmol) of methyl 2-oxo-1-pyrrolidineacetate and 11.4 g (81.4 mmol) of 7a-(aminomethyl)pyrrolizidine was heated and stirred for 6 hours at 80° C. under argon atmospher. After cooling, the reaction mixture was then solved with 1.0N-hydrochloric acid and extracted 3 times with dichloromethane. An aqueous layer was rendered alkaline by the addition of sodium hydroxide solution and extracted 3 times with dichloromethane followed by drying over anhydrous magnesium sulfate. After removal of the drying agent through filtration, the solvent was evaporated under reduced pressure to obtain a yellowish oil as a free base of the desired compound. The free base was converted to terephthalate by usual manner. Yield: 32.0 g (91.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04678801 |
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| Source dataset | uspto-grants-1987_07 |
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| ORD ID | ord-c737d048556d4021bb12fa503bcad00a |
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| Source note | uspto-grants-1987_07 |
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