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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052118Generated: November 1, 2026

Sodium Iodide → Dibenzyl (S)-2,5-dihydro-1H-pyrrole-1,2-dicarboxylate

https://huagongshe.com/reaction/1052118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactant(S)-2,5-Dihydro-pyrrole-1,2-dicarboxylic acid 1-benzyl esterHCID 10422063—
SolventDimethylformamideHCID 6228—
ProductDibenzyl (S)-2,5-dihydro-1H-pyrrole-1,2-dicarboxylateHCID 11142303—

Reaction Steps

To a solution of (S)-2,5-dihydro-pyrrole-1,2-dicarboxylic acid 1-benzyl ester (29.6 g, 120 mmol) in DMF (250 mL) were added cesium carbonate (42.9 g, 132 mmol) followed by benzyl bromide (17.09 mL, 144 mmol) and sodium iodide (2.15 g, 14.37 mmol) and the mixture was stirred at RT for 48 h. The reaction mixture was quenched with water (500 mL) and extracted with EtOAc (3×200 mL). The organic extracts were combined and washed with brine, dried (Na2SO4), filtered and concentrated. The crude residue was purified by flash column chromatography on silica gel (c-hexane/EtOAc 4:1) to give the desired material. MS (UPLC/MS): 338 [MH-Boc]+; tR (HPLC conditions b): 2.31 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388199B2
Source datasetuspto-grants-2016_07
ORD IDord-b35c9226983948cfa02c054a65a95f7e
Source noteuspto-grants-2016_07