Hydrochloric Acid → HCID 20030105, Verbindung

HRID 638004Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 638004
[C:1]([CH2:3][N:4]1[CH2:9][CH2:8][CH:7]([C:10](=[O:18])[C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[CH2:6][CH2:5]1)#[N:2].[ClH:19].[H][H]>C(O)(=O)C.[Pt]=O>[ClH:19].[NH2:2][CH2:1][CH2:3][N:4]1[CH2:5][CH2:6][CH:7]([C:10](=[O:18])[C:11]2[CH:12]=[CH:13][C:14]([F:17])=[CH:15][CH:16]=2)[CH2:8][CH2:9]1

Komponenten

6

Edukt 3

HCID 313Hydrochloric AcidHCID 30200424-(4-Fluorobenzoyl)piperidine-1-acetonitrileHCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 20030105HCID 20030105, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 82844Platinum oxide (PtO)KatalysatorHCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

14.1 g (0.05 mol) of N-(cyanomethyl)-4-(p-fluorobenzoyl)-piperidine are dissolved in 1.5 liters of glacial acetic acid and 30 ml of concentrated hydrochloric acid and hydrogenated together with 2 g of platinum oxide in a hydrogen atmosphere. After 6 hours, the theoretical amount of 2.25 liters of hydrogen is absorbed. The catalyst is then filtered off with suction and the filtrate is concentrated to approximately 30 ml in a water-jet vacuum. There is added to the resulting crystal mass 5 ml of isopropanol and 15 ml of ether and filtration with suction is carried out. After filtration with suction and drying, N-(2-aminoethyl)-4-(p-fluorobenzoyl)-piperidine hydrochloride is obtained which, after recrystallisation from methanol, melts at 265° with decomposition.

Aufarbeitung

  1. customthe theoretical amount of 2.25 liters of hydrogen is absorbed
  2. filtrationThe catalyst is then filtered off with suction
  3. concentrationthe filtrate is concentrated to approximately 30 ml in a water-jet vacuum
  4. additionThere is added to the resulting crystal mass 5 ml of isopropanol and 15 ml of ether and filtration with suction
  5. filtrationAfter filtration with suction
  6. customdrying

Quellen und Nachweise

ORD-Eintrag
ord-d88d9fd90de44b5fae36cb4b229aa33d
Quelldatensatz
uspto-grants-1985_12
Patentnummer
US04559349

Notizen zur Reaktion

Wird geladen…