Ammonium Acetate → 1-[(4-Methylphenyl)methyl]piperidin-4-amine

HRID 1059676

Reaktionsgleichung

Reaktionsgleichung von HRID 1059676
[CH3:1][C:2]1[CH:15]=[CH:14][C:5]([CH2:6][N:7]2[CH2:12][CH2:11][C:10](=O)[CH2:9][CH2:8]2)=[CH:4][CH:3]=1.C([O-])(=O)C.[NH4+].C([BH3-])#[N:22].[Na+]>CO>[CH3:1][C:2]1[CH:15]=[CH:14][C:5]([CH2:6][N:7]2[CH2:12][CH2:11][CH:10]([NH2:22])[CH2:9][CH2:8]2)=[CH:4][CH:3]=1

Komponenten

5

Edukt 3

HCID 517165Ammonium AcetateHCID 5003444Sodium cyanoborohydrideHCID 119595411-(4-Methylbenzyl)piperidin-4-one

Produkt 1

HCID 126418361-[(4-Methylphenyl)methyl]piperidin-4-amineAusbeute 48,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To 4.25 g (21 mmol) of 1-(4-methylbenzyl)-4-piperidinone 124 in 200 mL of anhydrous methanol was added 32.2 g (420 mmol) of ammonium acetate and 25 g of 3A molecular sieves. After stirring 30 min, 5.25 g (84 mmol) of sodium cyanoborohydride was added portionwise. After stirring 16 hours, the mixture was gravity filtered and the methanol evaporated under vacuum. The residue was partitioned between ether and ice/HCl. The acidic aqueous layer was extracted twice with ether, made basic with 50% aqueous NaOH and ice, and extracted with CH2Cl2 to give 2.1 g (48%) of the title amine 125 as a thick oil. GC/MS showed a molecular ion of 204. The product was used as is without further purification.

Aufarbeitung

  1. stirringAfter stirring 16 hours
  2. filtrationfiltered
  3. customthe methanol evaporated under vacuum
  4. customThe residue was partitioned between ether and ice/HCl
  5. extractionThe acidic aqueous layer was extracted twice with ether
  6. extractionextracted with CH2Cl2

Quellen und Nachweise

ORD-Eintrag
ord-5f661590bdc4477988b338af869038e5
Quelldatensatz
uspto-grants-2003_02
Patentnummer
US06521622B1

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