Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutyl 3,4-epoxybutyrate | HCID 5463767 | — |
| Reactant | 1,4-Diazaspiro[4.5]decan-2-one | HCID 13125039 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | Oxiracetam | HCID 4626 | — |
Reaction Steps
19 g 2-(1-Methylethyl)imidazolidinone ((5); R4 =H, R5 =isopropyl) (0.15 moles) are dissolved in 100 ml water and 150 ml acetone. 2-Methylpropyl-3,4-epoxybutanoate (0.15 moles) are added and the mixture is heated and stirred for 48 h at 70° C. The acetone is evaporated in vacuo and 100 ml DMF are added, followed by boiling for 21 h. The mixture is reduced to a small volume in vacuo, the residue is taken up with 40 ml water and washed with 2×40 ml methylene chloride. The aqueous phase is evaporated to dryness and redissolved in 15 ml methanol. This is left to stand for 3 h at 0° C., filtered and dried to give oxiracetam as a white crystalline powder, m.p. 167°-70° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04797496 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-49690035c3a04da091db851f55d062f6 |
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| Source note | uspto-grants-1989_01 |
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