Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 13534114 | HCID 13534114 | — |
| Reactant | HCID 13534115 | HCID 13534115 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 23324912 | HCID 23324912 | — |
| Product | HCID 23324927 | HCID 23324927 | — |
Reaction Steps
A solution of 93.4 g of 5-oxo-3-phenyl-2-pyrrolidinepropanoic acid methyl ester and 5-oxo-βphenyl-2-pyrrolidinepropanoic acid methyl ester in 370 ml of 1N aqueous sodium hydroxide solution is heated to 60° C. for four hours. Excess aqueous hydrochloric acid (1 N, 370 ml) is added and the solution is concentrated under reduced pressure to yield 5-oxo-β-phenyl-2-pyrrolidinepropanoic acid and 5-oxo-3-phenyl-2-pyrrolidinepropanoic acid. The acids are dissolved in 300 ml of acetic anyhydride and the solution heated to 90° C. The solution is filtered hot and the filtrate concentrated in vacuo. The oil is chromatographed on silica gel (200-400 mesh) to give cis- and trans-dihydro-1-phenyl-1H-pyrrolizine-3,5(2H,6H)-diones as a white solid with mp 151°-3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04584313 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-db096dc6b7084e9f95192b607cfef74c |
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| Source note | uspto-grants-1986_04 |
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