Epichlorohydrin → 4-(3-chloro-2-hydroxypropylamino)-N-methylphthalimide

HRID 1902397

Reaktionsgleichung

Reaktionsgleichung von HRID 1902397
[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[O:10])[N:8]([CH3:11])[C:6](=[O:7])[C:5]2=[CH:12][CH:13]=1.[Cl:14][CH2:15][CH:16]1[O:18][CH2:17]1>FC(F)(F)CO>[Cl:14][CH2:15][CH:16]([OH:18])[CH2:17][NH:1][C:2]1[CH:3]=[C:4]2[C:9](=[O:10])[N:8]([CH3:11])[C:6](=[O:7])[C:5]2=[CH:12][CH:13]=1

Komponenten

4

Edukt 2

HCID 7835EpichlorohydrinHCID 7269315-amino-2-methyl-2,3-dihydro-1H-isoindole-1,3-dione

Produkt 1

HCID 212817364-(3-chloro-2-hydroxypropylamino)-N-methylphthalimideAusbeute 77,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 64092,2,2-TrifluoroethanolLösungsmittel

Versuchsvorschrift

Twenty-five grams (g) (0.142 mole) 4-amino-N-methylphthalimide [Flitsch, Chem. Ber. 94:2494(1961)] and 20.7 g (0.21 mole) 1-chloro-2,3-epoxypropane were added to 150 ml 2,2,2-trifluoroethanol and the reaction mixture was heated to reflux with stirring for 48 hours. Seventy to eighty ml of 2,2,2-trifluoroethanol was removed by distillation and a heavy yellow precipitate formed when the remaining solution cooled to room temperature. This precipitate was triturated with ethyl acetate, collected by filtration and dried to give 29.5 g (77% yield) of the desired phthalimide intermediate m.p. 136°-138.5° C.

Aufarbeitung

  1. temperaturethe reaction mixture was heated
  2. temperatureto reflux
  3. customSeventy to eighty ml of 2,2,2-trifluoroethanol was removed by distillation
  4. customa heavy yellow precipitate formed when the remaining solution
  5. customThis precipitate was triturated with ethyl acetate
  6. filtrationcollected by filtration
  7. customdried

Quellen und Nachweise

ORD-Eintrag
ord-af7f62e27b714720a4f472f3c5901a3a
Quelldatensatz
uspto-grants-1982_12
Patentnummer
US04363759

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