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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277298Generated: October 30, 2026

Sodium Iodide → HCID 22601787, compound

https://huagongshe.com/reaction/277298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantBenzonitrile, 3-(bromomethyl)-HCID 97249—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
ReactantSodium BicarbonateHCID 516892—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 22601787HCID 22601787—

Reaction Steps

m-Cyanobenzyl bromide (2.35 g, 12.0 mmol) was slowly added to a solution of glycine methyl ester hydrochloride (0.63 g, 5.0 mmol), NaHCO3 (1.4 g, 17.0 mmol) and NaI (0.37 g, 2.4 mmol) in DMSO (5 mL) and THF (20 mL). The reaction was heated to reflux for 2 hours, cooled to room temperature and diluted with EtOAc (50 ml) and water (40 mL). The organic phase was washed with water (3×40 mL), saturated aqueous NaCl (40 mL), dried (Na2SO4), filtered and concentrated in vacuo to give N,N-Bis(m-cyanobenzyl)glycine methyl ester as a colorless oil of sufficient purity for subsequent reactions. Additional purification can be achieved by extraction into dilute aqueous acid, basification and extraction in an organic solvent. 1H NMR (200 MHz, CDCl3): δ3.39, s, 2H; 3.71, s, 3H; 3.86, s, 4H; 7.39-7.73, m, 10H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355683B1
Source datasetuspto-grants-2002_03
ORD IDord-189ce99fac1343b1bee9aee0c998f3e2
Source noteuspto-grants-2002_03