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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
ReactantMethyl 1-benzyl-5-oxo-2-pyrrolidinecarboxylateHCID 11096495—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 1-benzyl-5-thioxo-2-pyrrolidinecarboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129235B2
Source datasetuspto-grants-2006_10
ORD IDord-7ce1823af5d1458a989ee67746ba90e2
Source noteuspto-grants-2006_10