HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246699Generated: October 26, 2026
Lawesson's reagent → Methyl 1-benzyl-5-thioxo-2-pyrrolidinecarboxylate
https://huagongshe.com/reaction/1246699
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | Methyl 1-benzyl-5-oxo-2-pyrrolidinecarboxylate | HCID 11096495 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 1-benzyl-5-thioxo-2-pyrrolidinecarboxylate | HCID 14759675 | — |
Reaction Steps
Methyl 1-benzyl-5-oxo-2-pyrrolidinecarboxylate (18.15 g, 77.8 mmol) and Lawesson's reagent (31.5 g, 77.9 mmol) were combined in dry tetrahydrofuran (100 mL) and stirred overnight at room temperature. The mixture was filtered, the filter cake was rinsed with tetrahydrofuran, and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and washed with saturated sodium bicarbonate solution. The organic phase was concentrated under reduced pressure and the residue was purified by chromatography on silica gel (3:1, hexanes:ethyl acetate) to provide the title compound. MS (ESI) m/z: 250 (M+H)+; 1H NMR (CDCl3) δ 2.17 (m, 1H), 2.27 (m, 1H), 3.15 (m, 2H), 3.69 (s, 3H), 4.30 (dd, 1H), 4.37 (d, 1H), 5.73 (d, 1H), 7.32 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129235B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-7ce1823af5d1458a989ee67746ba90e2 |
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| Source note | uspto-grants-2006_10 |
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