Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Succinimide | HCID 11439 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium metaborate | HCID 145326 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Product | 5-Ethoxy-2-pyrrolidinone | HCID 3580555 | 55% |
Reaction Steps
At 0° C., 9.91 g of succinimide were charged initially in 415 ml of ethanol and a total of 5.53 g of sodium boranate was added a little at a time. At this temperature, every 15 minutes 2 to 3 drops of 2N ethanolic hydrogen chloride were added dropwise over 4½ hours. Subsequently, the mixture was acidified to pH 3 using more acid. After stirring for 1 hour at 0° C., the mixture was neutralized using 1% strength ethanolic potassium hydroxide solution and the mixture was stirred for a further 15 minutes and evaporated. The residue was taken up in water and extracted three times with dichloromethane. After drying over sodium sulphate and concentrating, 7.16 g (55% of theory) of γ-ethoxy-γ-butyrolactam were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06274613B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-9a954078d2b940cfa340074bf2d486c1 |
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| Source note | uspto-grants-2001_08 |
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