Réaction #792141

ord-855ed5f194584302be2c3940b738ae72

Équation de réaction

[BH3-]C#N.[Na+]
sodium cyanoborohydride
CC(=O)O
acetic acid
CC(=O)C1Cc2ccccc2C1
1-(indan-2-yl)ethanone
NC1CC1
cyclopropylamine
CC(NC1CC1)C1Cc2ccccc2C1
N-[1-(indan-2-yl)ethyl]cyclopropanamine
Rendement 28.0%

Solvants

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températureat reflux
  2. 2
    workup.STIRRINGthe reaction mixture is further stirred for 2 hrs
  3. 3
    Températureat reflux
  4. 4
    AutreThe cooled reaction mixture
  5. 5
    Filtrationis then filtered over a cake of diatomaceous earth
  6. 6
    LavageThe cake is washed twice by 80 ml of methanol
  7. 7
    Concentrationthe combined methanolic extracts are concentrated under vacuum
  8. 8
    workup.ADDITION100 ml of water are then added to the residue
  9. 9
    ExtractionThe watery layer is extracted with 300 ml of ethyl acetate
  10. 10
    LavageThe organic layer is washed twice by brine
  11. 11
    Filtrationfiltered over a phase separator paper
  12. 12
    Autreto yield after concentration 5 g of a yellow oil

Mode opératoire

To a cooled solution of 3.5 g (21.8 mmol) of 1-(indan-2-yl)ethanone in 100 ml of methanol, are added 10 g of 3 Å molecular sieves and 2.3 g (40.2 mmol) of cyclopropylamine followed by a slow addition of 2.87 ml (50.2 mmol) of acetic acid. The reaction mixture is stirred for 2.5 hrs at reflux. The reaction mixture is then cooled to 0° C. and 1.9 g (30 mmol) of sodium cyanoborohydride are slowly added and the reaction mixture is further stirred for 2 hrs at reflux. The cooled reaction mixture is then filtered over a cake of diatomaceous earth. The cake is washed twice by 80 ml of methanol and the combined methanolic extracts are concentrated under vacuum. 100 ml of water are then added to the residue and the pH is ajusted to 12 with a 0.5 N solution of sodium hydroxyde. The watery layer is extracted with 300 ml of ethyl acetate. The organic layer is washed twice by brine and filtered over a phase separator paper to yield after concentration 5 g of a yellow oil. Column chromatography on silica gel (gradient heptane/ethyl acetate) yields 1.2 g (28% yield) of N-[1-(indan-2-yl)ethyl]cyclopropanamine as a colourless oil (M+H =202).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09173399B2uspto-grants-2015_11