Ammonia → (+/-)-cis-6-(2-Aminoethyl)-1,3-dioxane-4acetic acid

HRID 893502Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 893502
[C:1]([CH2:3][C@H:4]1[O:9][CH2:8][O:7][C@@H:6]([CH2:10][C:11]([OH:13])=[O:12])[CH2:5]1)#[N:2].N.O.[H][H]>CO>[NH2:2][CH2:1][CH2:3][C@H:4]1[O:9][CH2:8][O:7][C@@H:6]([CH2:10][C:11]([OH:13])=[O:12])[CH2:5]1

Komponenten

6

Reaktionsbedingungen

Temperatur
45 °C

Versuchsvorschrift

A solution of 1.04 g (4.88 mmol) of (±)-cis-6-(cyanomethyl)-1,3-dioxane-4-acetic acid in 100 mL of methanol saturated with anhydrous ammonia is added to PG,75 a Parr shaker bottle Containing 0.53 g of water wet Raney nickel #30. The solution is heated at 45° C. and 50 pounds per square inch gage (psig) hydrogen pressure for 17 hours. The suspension is cooled and filtered to remove the Raney nickel through filter aid and the precipitate washed with methanol. The filtrate is concentrated at reduced pressure. The residue is dissolved in methanol saturated with anhydrous ammonia, treated with decolorizing charcoal, filtered through filter aid and evaporated to give 0.56 g of (±)-cis-6-(2-aminoethyl)-1,3-dioxane-4-acetic acid.

Aufarbeitung

  1. temperatureThe suspension is cooled
  2. filtrationfiltered
  3. customto remove the Raney nickel
  4. filtrationthrough filter aid
  5. washthe precipitate washed with methanol
  6. concentrationThe filtrate is concentrated at reduced pressure
  7. dissolutionThe residue is dissolved in methanol saturated with anhydrous ammonia
  8. additiontreated with decolorizing charcoal
  9. filtrationfiltered
  10. filtrationthrough filter aid
  11. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-af72071c8ad948479445e46986ab4795
Quelldatensatz
uspto-grants-1992_06
Patentnummer
US05124482

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