Ethyl cyanoacetate → 2-cyano-N-(4-methylbenzyl)acetamide

HRID 2418974Notes

Reaction equation

HRID 2418974 reaction equation
[C:1]([CH2:3][C:4]([O:6]CC)=O)#[N:2].[CH3:9][C:10]1[CH:17]=[CH:16][C:13]([CH2:14][NH2:15])=[CH:12][CH:11]=1>COCCO>[CH3:9][C:10]1[CH:17]=[CH:16][C:13]([CH2:14][NH:15][C:4](=[O:6])[CH2:3][C:1]#[N:2])=[CH:12][CH:11]=1

Participants

4

Procedure

A solution of 93 g. (0.825 mole) of ethyl cyanoacetate and 100 g. (0.825 mole) of 4-methylbenzylamine in 150 ml. of 2-methoxyethanol is refluxed for 2 hr. After cooling the solid product is isolated by vacuum filtration, washed with pentane and dried to give 90 g. (57.6%) of amide as a white solid: m.p. 124°-6° C.;ν3220 (NH), 2230 (CN), and 1630 cm.-1 (C= O)δ8.77 broad, 1H, NH); 7.17 (s, 4H, phenyl protons), 4.28 (d, 2H, benzyl methylene), 3.67 (s, 2H, CH2CO), and 2.28 (s, 3H, CH3).

Workup

  1. temperatureAfter cooling the solid product
  2. customis isolated by vacuum filtration
  3. washwashed with pentane
  4. customdried
  5. customto give 90 g

Sources & evidence

ORD record
ord-5239ee6f6f9e464b815590a69b01d841
Source dataset
uspto-grants-1978_08
Patent number
US04104273

Reaction notes

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