1-Benzyl-4-(methoxymethyl)-N-phenylpiperidin-4-amine → 4-(Methoxymethyl)-N-phenylpiperidin-4-amine

HRID 28161Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 28161
[CH3:1][O:2][CH2:3][C:4]1([NH:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH2:9][CH2:8][N:7](CC2C=CC=CC=2)[CH2:6][CH2:5]1.[H][H]>[Pd].C(O)(=O)C>[CH3:1][O:2][CH2:3][C:4]1([NH:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH2:9][CH2:8][NH:7][CH2:6][CH2:5]1

Komponenten

5

Edukt 2

HCID 30477241-Benzyl-4-(methoxymethyl)-N-phenylpiperidin-4-amineHCID 178418361HCID 178418361, Verbindung

Produkt 1

HCID 183199324-(Methoxymethyl)-N-phenylpiperidin-4-amine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

A mixture of 10 parts of 4-(methoxymethyl)-N-phenyl-1-(phenylmethyl)-4-piperidinamine and 200 parts of acetic acid is hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. The oily residue is dissolved in water, cooled and alkalized with ammonium hydroxide. The product is extracted with trichloromethane. The extract is washed with water, dried, filtered and evaporated. The oily residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) saturated with gaseous ammonia, as eluent. The pure fractions are collected and the eluent is evaporated, yielding 4.5 parts of 4-(methoxymethyl)-N-phenyl-4-piperidinamine as an oily residue.

Aufarbeitung

  1. filtrationthe catalyst is filtered off
  2. customthe filtrate is evaporated
  3. dissolutionThe oily residue is dissolved in water
  4. temperaturecooled
  5. extractionThe product is extracted with trichloromethane
  6. washThe extract is washed with water
  7. customdried
  8. filtrationfiltered
  9. customevaporated
  10. customThe oily residue is purified by column-chromatography over silica gel using
  11. additiona mixture of trichloromethane and methanol (90:10 by volume) saturated with gaseous ammonia
  12. customThe pure fractions are collected
  13. customthe eluent is evaporated

Quellen und Nachweise

ORD-Eintrag
ord-c5fc458971034ceab82186d593e9b786
Quelldatensatz
uspto-grants-1980_09
Patentnummer
US04225606

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