Chloroacetonitrile → HCID 20225324, compound

HRID 463674

Reaction equation

HRID 463674 reaction equation
[CH2:1]([NH:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])[CH3:2].Cl[CH2:12][C:13]#[N:14].C(=O)([O-])[O-].[Na+].[Na+]>C1(C)C=CC=CC=1>[CH2:1]([N:3]([CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])[CH2:12][C:13]#[N:14])[CH3:2]

Participants

5

Conditions

Temperature
125 °C

Procedure

Combine 7.95 g (0.055 moles) ethyl(heptyl)amine, 3.5 ml (0.055 moles) chloroacetonitrile, 5.8 g (0.055 moles) sodium carbonate and 25 ml toluene in a sealed pressure tube. Heat to 125° C. for 18 hrs. Follow the progress of the reaction by thin layer chromatography on silica gel (CH3CN+MeOH+NH4OH, 85+10+5). At the completion of the reaction, filter the reaction mixture and evaporate the solvents to provide the title compound.

Workup

  1. customthe progress of the reaction by thin layer chromatography on silica gel (CH3CN+MeOH+NH4OH, 85+10+5)
  2. customAt the completion of the reaction
  3. filtrationfilter the reaction mixture
  4. customevaporate the solvents

Sources & evidence

ORD record
ord-848d384f4a9e4071b0ce402d368bbeaf
Source dataset
uspto-grants-1985_10
Patent number
US04544654

Linked notes

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