Dimethylformamide dimethyl acetal → Ethyl 3-(dimethylamino)-2-isocyanoacrylate

HRID 1532243Notes

Reaction equation

HRID 1532243 reaction equation
[N+:1]([CH2:3][C:4]([O:6][CH2:7][CH3:8])=[O:5])#[C-:2].CO[CH:11](OC)[N:12]([CH3:14])[CH3:13]>C(O)C>[CH2:7]([O:6][C:4](=[O:5])[C:3]([N+:1]#[C-:2])=[CH:11][N:12]([CH3:14])[CH3:13])[CH3:8]

Participants

4

Procedure

To a solution of ethyl isocyanoacetate (5.0 g) in ethanol (100 mL) is added N,N-dimethyl-formamide dimethyl acetal (6.5 g) dropwise with stirring over 10 minutes. The reaction is stirred for 24 hours and the ethanol is evaporated. The resulting oil is passed through magnesium silicate using 50% ethyl acetate-hexanes as the eluant. The solvents are removed and the resulting oil is crystallized from ethyl acetate-hexanes to yield light yellow needles, 3.0 g.

Workup

  1. stirringThe reaction is stirred for 24 hours
  2. customthe ethanol is evaporated
  3. customThe solvents are removed
  4. customthe resulting oil is crystallized from ethyl acetate-hexanes
  5. customto yield light yellow needles, 3.0 g

Sources & evidence

ORD record
ord-aa2db32c9d7848a9b8cd142a55dd8c4f
Source dataset
uspto-grants-2001_03
Patent number
US06201013B1

Reaction notes

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