HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029672Generated: October 31, 2026
Benzyl Bromide → (S)-Methyl 1-benzyl-5-oxopyrrolidine-2-carboxylate
https://huagongshe.com/reaction/1029672
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 5-oxo-L-prolinate | HCID 78646 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-Methyl 1-benzyl-5-oxopyrrolidine-2-carboxylate | HCID 10998904 | — |
Reaction Steps
To a solution of methyl (2S)-5-pyrrolidone-2-carboxylate (80 g) in tetrahydrofuran (900 ml) was added sodium hydride (60% in oil, 23.5 g) by portions. After the addition, the reaction mixture was heated to 60° C., and benzyl bromide (69.8 ml) was added dropwise thereto. After 3 hours, the reaction mixture was cooled to room temperature and water (100 ml) was added dropwise thereto. The reaction mixture was poured into a mixture of ethyl acetate (2 l) and water (800 ml). The organic layer was separated, washed with brine, and dried over magnesium sulfate. Evaporation of the solvent gave an oil, which was chromatographed on silica gel (2 l) eluting with a mixture of hexane and ethyl acetate (1:1→1:2, V/V) to give methyl (2S)-1-benzyl-5-pyrrolidone-2-carboxylate (100.8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05102877 |
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| Source dataset | uspto-grants-1992_04 |
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| ORD ID | ord-41ffd208cacf43a09e64464f05c3fe32 |
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| Source note | uspto-grants-1992_04 |
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