Sodium Iodide → HCID 22601787, compound

HRID 277298Notes

Reaction equation

HRID 277298 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][CH:10]=1)[CH2:6]Br)#[N:2].Cl.[CH3:12][O:13][C:14](=[O:17])[CH2:15][NH2:16].C([O-])(O)=O.[Na+].[Na+].[I-]>CS(C)=O.C1COCC1.CCOC(C)=O.O>[CH3:12][O:13][C:14](=[O:17])[CH2:15][N:16]([CH2:6][C:5]1[CH:8]=[CH:9][CH:10]=[C:3]([C:1]#[N:2])[CH:4]=1)[CH2:6][C:5]1[CH:8]=[CH:9][CH:10]=[C:3]([C:1]#[N:2])[CH:4]=1

Participants

9

Procedure

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.

Workup

  1. temperatureThe reaction was heated
  2. temperatureto reflux for 2 hours
  3. washThe organic phase was washed with water (3×40 mL), saturated aqueous NaCl (40 mL)
  4. dry with materialdried (Na2SO4)
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-189ce99fac1343b1bee9aee0c998f3e2
Source dataset
uspto-grants-2002_03
Patent number
US06355683B1

Reaction notes

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