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Ethanol → HCID 178437743, Verbindung

HRID 1356529
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1356529
[NH4+].Cl[C:3]1[N:8]=[C:7]([OH:9])[C:6]([F:10])=[C:5]([CH2:11][CH3:12])[N:4]=1.C(O)C>[Pd].O>[CH2:11]([C:5]1[N:4]=[CH:3][N:8]=[C:7]([OH:9])[C:6]=1[F:10])[CH3:12]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 702EthanolHCID 178437663HCID 178437663, Verbindung

Produkt 1

HCID 178437743HCID 178437743, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 962WaterLösungsmittel2×

Reaktionsbedingungen

Temperatur
4 °C

Versuchsvorschrift

To a mixture of the compound of part (iii) (34 kg), ethanol (170 L) and water (5 kg) was added 5% w/w palladium-on-carbon (50% w/w water content) (3.4 kg) and the mixture hydrogenated at 50° C. and 345 kPa (50 psi) until completion of the reaction. Water (10.5 L) w as added and the catalyst removed by filtration. The filtrate was concentrated under reduced pressure to a small volume and extracted with dichloromethane (2×58 L). The combined organic extracts were concentrated under reduced pressure and toluene (150 L) added. The mixture was concentrated under reduced pressure to 50 L in volume, toluene (50 L) added and cooled to 4° C. for 4 hours. The precipitated product was collected by filtration, washed with toluene (10 L) and dried (Yield=20 kg), m.p. 112-4° C.

Aufarbeitung

  1. customthe mixture hydrogenated at 50° C. and 345 kPa (50 psi) until completion of the reaction
  2. customthe catalyst removed by filtration
  3. concentrationThe filtrate was concentrated under reduced pressure to a small volume
  4. extractionextracted with dichloromethane (2×58 L)
  5. concentrationThe combined organic extracts were concentrated under reduced pressure and toluene (150 L)
  6. additionadded
  7. concentrationThe mixture was concentrated under reduced pressure to 50 L in volume, toluene (50 L)
  8. additionadded
  9. filtrationThe precipitated product was collected by filtration
  10. washwashed with toluene (10 L)
  11. customdried (Yield=20 kg), m.p. 112-4° C.

Quellen und Nachweise

ORD-Eintrag
ord-773220c0a00e4dea848ca95d1febd439
Quelldatensatz
uspto-grants-2003_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06586594B1

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