Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cerium(III) chloride | HCID 24636 | — |
| Reactant | benzyl (2S)-2-methyl-3-oxopyrrolidine-1-carboxylate | HCID 59556933 | — |
| Reactant | HCID 178467822 | HCID 178467822 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59557026 | HCID 59557026 | 84% |
Reaction Steps
A suspension (300 mL) of cerium chloride (47 g) in THF was cooled to −78° C., and 3 mol/L methylmagnesium bromide-diethyl ether solution (56 mL) was added dropwise while adjusting the temperature of the solution to not higher than −70° C. After the completion of the dropwise addition, the mixture was stirred at −78° C. for 30 min, and a solution (60 mL) of benzyl (2S)-2-methyl-3-oxopyrrolidine-1-carboxylate (18 g) in THF was added dropwise while adjusting the temperature of the solution to not higher than −70° C. The reaction mixture was warmed to 0° C. over 2 hr, ethyl acetate (1 L) was added, and the insoluble material was filtered off. Water was added to the filtrate and then the mixture was partitioned. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=9/1→1/1) to give the title compound as a colorless oil (yield: 16.2 g, yield: 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08013008B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-5019fcd52eeb4ddc8df167a380e9185c |
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| Source note | uspto-grants-2011_09 |
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