Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Succinimide | HCID 11439 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Product | 5-Ethoxy-2-pyrrolidinone | HCID 3580555 | 55% |
Reaction Steps
At 0° C., 9.91 g of succinimide were initially charged in 415 ml of ethanol and admixed, a little at a time, with a total of 5.53 g of sodium borohydride. At this temperature, every 15 minutes 2 to 3 drops of 2N ethanolic hydrogen chloride were added dropwise over a period of 4½ hours. The mixture was subsequently acidified to pH 3 using more acid. The mixture was stirred at 0° C. for one hour and then neutralized with 1% strength ethanolic potassium hydroxide solution, stirred for a further 15 minutes and concentrated. The residue was taken up in water and extracted three times with dichloromethane. Drying over sodium sulphate and concentration gave 7.16 g (55% of theory) of γ-ethoxy-γ-butyrolactam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06632833B1 |
|---|
| Source dataset | uspto-grants-2003_10 |
|---|
| ORD ID | ord-368d9813843f4527bee5dabcf5087daa |
|---|
| Source note | uspto-grants-2003_10 |
|---|