Water → [Amino(ethoxy)methylidene]propanedinitrile

HRID 1439318Notes

Reaction equation

HRID 1439318 reaction equation
[C:1]([C-:3]([C:6]#[N:7])[C:4]#[N:5])#[N:2].[K+].O.[CH2:10]([O:12]CC)[CH3:11].S(=O)(=O)(O)O>C(O)C>[NH2:2][C:1]([O:12][CH2:10][CH3:11])=[C:3]([C:6]#[N:7])[C:4]#[N:5]

Participants

6

Procedure

A mixture of 12.9 g of potassium tricyanomethanide from I B, 40 ml of water and 120 ml of diethyl ether was cooled to 5°. To this mixture was added 10 g of concentrated sulfuric acid dropwise at such a rate as to keep the reaction mixture temperature below 10°. Upon complete addition of sulfuric acid, the reaction mixture was stirred during 20 minutes. The mixture was then placed in a separatory funnel and the middle layer drawn off to be used in the next reaction. To 50 ml of the solution from above was added 150 ml of ethanol and volatile material was removed until the boiling temperature exceeded 50°, when the mixture was heated to reflux. The mixture was maintained at the reflux temperature for 15 hours. The white slurry was cooled to 10°, and the solid collected by filtration to give 6.5 g of 3-amino-3-ethoxy-2-cyano-2-propenenitrile, m.p. 233°. A small sample was recrystallized from ethanol without change of melting point. the nmr spectrum was consistent with the assigned structure.

Workup

  1. temperaturewas cooled to 5°
  2. customthe reaction mixture temperature below 10°
  3. customThe mixture was then placed in a separatory funnel
  4. customto be used in the next reaction
  5. customwas removed until the boiling temperature
  6. customexceeded 50°
  7. temperaturewhen the mixture was heated to reflux
  8. temperatureThe mixture was maintained at the reflux temperature for 15 hours
  9. temperatureThe white slurry was cooled to 10°
  10. filtrationthe solid collected by filtration

Sources & evidence

ORD record
ord-715824b556e845edaf0a98f59015e2c4
Source dataset
uspto-grants-1977_11
Patent number
US04059433

Reaction notes

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