Dimethylformamide → HCID 54137088, compound

HRID 1112619Notes

Reaction equation

HRID 1112619 reaction equation
[C:1]([O:8][CH3:9])(=[O:7])/[CH:2]=[CH:3]\[C:4]([O-:6])=[O:5].[Na+].[C:11]1([CH2:17][C:18]#[N:19])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.CN(C)C=O>>[C:18]([CH:17]([CH:2]([CH2:3][C:4]([OH:6])=[O:5])[C:1]([O:8][CH3:9])=[O:7])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)#[N:19]

Participants

4

Reactant 3

HCID 6228DimethylformamideHCID 8794PhenylacetonitrileHCID 23681663Sodium methyl maleate

Product 1

HCID 54137088HCID 54137088, compoundYield 88%

Procedure

Into a 200 ml, one-neck flask is placed 35 grams of sodium methyl maleate (0.23 moles), 85 grams (0.73 moles) of phenyl acetonitrile and 80 g(1.1 moles) dimethyl formamide. The reaction mixture is heated to 135°-140° C. for 5 hours and then distilled in vacuo. The residue is extracted three times with 300 ml ether. The solid (56 grams) is then dissolved in water and acidified with 23 grams conc. HCl in 50 mls water. The liquid that separates out is dissolved in ether and washed with water to remove unreacted starting materials. The ether is distilled off to give a residue of 50 grams of product (yield: 88%). The structure is verified by NMR (in CDCl3):

Workup

  1. temperatureThe reaction mixture is heated to 135°-140° C. for 5 hours
  2. distillationdistilled in vacuo
  3. extractionThe residue is extracted three times with 300 ml ether
  4. dissolutionThe solid (56 grams) is then dissolved in water
  5. dissolutionThe liquid that separates out is dissolved in ether
  6. washwashed with water
  7. customto remove unreacted
  8. distillationThe ether is distilled off

Sources & evidence

ORD record
ord-b67489a1470a44d3a828ac0ab6c6d2ce
Source dataset
uspto-grants-1978_10
Patent number
US04123458

Reaction notes

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