Formaldehyde → HCID 21290608, Verbindung

HRID 623204Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 623204
[ClH:1].Cl.[C:3]1([CH:9]([CH2:12][NH2:13])[CH2:10][NH2:11])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[OH-].[Na+].[CH2:16]=O>O>[ClH:1].[ClH:1].[C:3]1([CH:9]2[CH2:10][NH:11][CH2:16][NH:13][CH2:12]2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

Komponenten

5

Versuchsvorschrift

37.5 g (0.168 mol) of 2-phenylpropane-1,3-diamine dihydrochloride are dissolved in 100 ml of water, and 13.52 g (0.336 mol) of sodium hydroxide pellets are added. The mixture is cooled in a bath of water+ice and 17 ml of a 30% (w/v) aqueous solution of formaldehyde are added. The mixture is left overnight at room temperature (15°-20° C.) and extracted with 5×50 ml of CHCl3, and the chloroform phase is washed with 25 ml of water, dried over MgSO4 and filtered. The filtrate is evaporated to dryness, the evaporation residue is taken up with 500 ml of anhydrous C2H5OH and acidified with ethanol containing HCl, and the precipitate formed is collected by filtration, washed with a small quantity of anhydrous ethanol and dried in vacuo to give 24 g (yield: 58%) of CRL 41 365. M.p. (inst.)=192° C.

Aufarbeitung

  1. additionare added
  2. extractionextracted with 5×50 ml of CHCl3
  3. washthe chloroform phase is washed with 25 ml of water
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. customThe filtrate is evaporated to dryness
  7. additioncontaining HCl
  8. customthe precipitate formed
  9. filtrationis collected by filtration
  10. washwashed with a small quantity of anhydrous ethanol
  11. customdried in vacuo
  12. customto give 24 g (yield: 58%) of CRL 41 365
  13. customM.p. (inst.)=192° C.

Quellen und Nachweise

ORD-Eintrag
ord-7ccc3113502444ca98e6c1cf11b98d35
Quelldatensatz
uspto-grants-1988_09
Patentnummer
US04774248

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