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Formaldehyde → 2-(Hydroxymethyl)-4,4-dimethyl-1-phenylpyrazolidin-3-one

HRID 1248164
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1248164
[CH3:1][C:2]1([CH3:14])[CH2:6][N:5]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[NH:4][C:3]1=[O:13].[CH2:15]=[O:16].C1(C)C=CC=CC=1>C(O)(=O)C>[CH3:1][C:2]1([CH3:14])[CH2:6][N:5]([C:7]2[CH:8]=[CH:9][CH:10]=[CH:11][CH:12]=2)[N:4]([CH2:15][OH:16])[C:3]1=[O:13]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 712FormaldehydeHCID 1140TolueneHCID 75861Dimezone

Produkt 1

HCID 3143062-(Hydroxymethyl)-4,4-dimethyl-1-phenylpyrazolidin-3-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

4,4-Dimethyl-1-phenyl-3-pyrazolidone (152 g) was dissolved in 600 ml of acetic acid. To the solution as prepared above, 97 g of an aqueous solution containing 37% of formaldehyde was dropped with stirring at room temperature. The resultant mixture was stirred for 2 hours. At the end of the time, the solvent was distilled away under reduced pressure. To the residue thus obtained, 100 ml of toluene was added, and water was separated at the toluene azeotrope under reduced pressure. A mixture of 900 ml of hexane and 700 ml of ethyl acetate was added to the residue as obtained above which was then dissolved therein by heating. The resultant solution was allowed to cool to room temperature. Crystals precipitated were collected by filtration to obtain 120 g of 4,4-dimethyl-2-hydroxymethyl-1-phenyl-3-pyrazolidone.

Aufarbeitung

  1. additionwas dropped
  2. distillationAt the end of the time, the solvent was distilled away under reduced pressure
  3. customTo the residue thus obtained
  4. customwater was separated at the toluene azeotrope under reduced pressure
  5. additionA mixture of 900 ml of hexane and 700 ml of ethyl acetate
  6. additionwas added to the residue
  7. customas obtained above which
  8. dissolutionwas then dissolved
  9. temperatureby heating
  10. temperatureto cool to room temperature
  11. customCrystals precipitated
  12. filtrationwere collected by filtration

Quellen und Nachweise

ORD-Eintrag
ord-da434442b82143ab9800d96fab40c1e9
Quelldatensatz
uspto-grants-1985_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04522917

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