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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660751Generated: October 28, 2026

Sodium Iodide → HCID 68842371, compound

https://huagongshe.com/reaction/660751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant4-BromobutyronitrileHCID 21412—
ReactantTri-o-tolylphosphineHCID 80271—
Reactant5-(2-Benzyloxy-4-iodophenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-oneHCID 66756937—
CatalystZincHCID 23994—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
ProductHCID 68842371HCID 68842371—

Reaction Steps

To a solution of 4-bromobutyronitrile (0.074 mL, 0.75 mmol) in DMF (2 mL) is added Rieke zinc (0.9 mmol) and a catalytic amount of NaI. The mixture is stirred at RT for 5 h then P(o-tolyl)3 (22.8 mg, 15 mol %), Pd2(dba)3 (13.7 mg, 3 mol %) and 5-(2-benzyloxy-4-iodophenyl)-1,1-dioxo-2-(2-trimethylsilanylethyl)-1,2,5-thiadiazolidin-3-one (272 mg, 0.5 mmol) is added and the mixture is stirred at RT for 18 h. The mixture is partitioned between EtOAc and 1N HCl and the organic phase is washed with brine and dried over sodium sulfate. The solvent is removed under reduced pressure and the residue is purified by column chromatography using a gradient of 0-15% EtOAc/hexane as eluent to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084448B2
Source datasetuspto-grants-2011_12
ORD IDord-6d1ae8e9abf847bcb5fb879884cf446f
Source noteuspto-grants-2011_12