Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | HCID 10016782 | HCID 10016782 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57680530 | HCID 57680530 | 82.1% |
Reaction Steps
To a solution of (S)-1-tert-butyl 2-ethyl 4,4-dimethyl-5-oxopyrrolidine-1,2-dicarboxylate (163D) (10 g, 0.035 mol) in dry THF (60 mL) stirred at −78° C. under nitrogen was added a 1 M solution of lithium hexmethyldisilazide in THF (38.5 mL, 0.038 mol). The mixture was stirred at −78° C. for 30 min, iodomethane (5.4 g, 0.038 mol) in THF (5 mL) was added, and the mixture was then stirred 1 h, warmed up to room temperature and continued stirring for additional 3 h. The reaction mixture was quenched with saturated ammonium chloride solution and extracted with CH2Cl2 (3×100 mL). The combined organic layers were dried over Na2SO4, filtered, and evaporated to dryness. The residue was purified by flash chromatography (10-20% EtOAc/hexanxe) to furnish (163E) (8.2 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592579B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-7735be9e1dea4bed9020d806da68ab58 |
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| Source note | uspto-grants-2013_11 |
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